A síndrome de Hipertermia Maligna, Artrogripose e Torcicolo é uma condição de artrogripose extremamente rara, descrita até hoje em apenas dois pares de irmãos de duas famílias não relacionadas. Ela se caracteriza pela combinação de: enrijecimento das articulações presente desde o nascimento (artrogripose), torcicolo congênito, traços faciais incomuns (como um lado do rosto diferente do outro, movimentos fracos dos músculos faciais, pálpebra caída, orelhas posicionadas mais para trás e céu da boca aberto), curvatura progressiva da coluna (escoliose) e episódios de superaquecimento perigoso do corpo (hipertermia maligna). Desde 1988, não foram registradas outras descrições na literatura médica.
Introdução
O que você precisa saber de cara
A síndrome de Hipertermia Maligna, Artrogripose e Torcicolo é uma condição de artrogripose extremamente rara, descrita até hoje em apenas dois pares de irmãos de duas famílias não relacionadas. Ela se caracteriza pela combinação de: enrijecimento das articulações presente desde o nascimento (artrogripose), torcicolo congênito, traços faciais incomuns (como um lado do rosto diferente do outro, movimentos fracos dos músculos faciais, pálpebra caída, orelhas posicionadas mais para trás e céu da boca aberto), curvatura progressiva da coluna (escoliose) e episódios de superaquecimento perigoso do corpo (hipertermia maligna). Desde 1988, não foram registradas outras descrições na literatura médica.
Escala de raridade
<1/50kMuito rara
1/20kRara
1/10kPouco freq.
1/5kIncomum
1/2k
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Sinais e sintomas
O que aparece no corpo e com que frequência cada sintoma acontece
Partes do corpo afetadas
+ 28 sintomas em outras categorias
Características mais comuns
Os sintomas variam de pessoa para pessoa. Abaixo estão as 66 características clínicas mais associadas, ordenadas por frequência.
Linha do tempo da pesquisa
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Genética e causas
O que está alterado no DNA e como passa nas famílias
Nenhum gene associado encontrado
Os dados genéticos desta condição ainda estão sendo catalogados.
Diagnóstico
Os sinais que médicos procuram e os exames que confirmam
Tratamento e manejo
Remédios, cuidados de apoio e o que precisa acompanhar
Onde tratar no SUS
Hospitais de referência no Brasil e o protocolo oficial do SUS (PCDT)
🇧🇷 Atendimento SUS — Síndrome de pterígio múltiplo-hipertermia maligna
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Pesquisa ativa
Ensaios clínicos abertos e novidades científicas recentes
Pesquisa e ensaios clínicos
Nenhum ensaio clínico registrado para esta condição.
Publicações mais relevantes
The Clinical, Histological, and Genetic Spectrum of RYR1 Variants-A Multi-Center Israeli Cohort Study.
Background: Variants in the ryanodine receptor 1 (RYR1) gene have been linked to a range of disorders, from congenital myopathy to adult-onset manifestations, with phenotypes varying from mild to severe. Methods: A retrospective review was conducted on an Israeli cohort of 36 individuals with RYR1 variants, identified through genetic testing as part of a national collaboration among multiple pediatric and adult neuromuscular clinics. Clinical features, molecular data, laboratory results, electromyographic findings, and muscle histology were analyzed. Each variant was classified according to its respective domain within the RYR1 gene. Results: Thirty-six cases were included in the analysis; 31 were from 11 unrelated families, and 5 were sporadic. Nine individuals were asymptomatic with normal CK levels. Most of the 27 affected patients presented with variable degrees of perinatal weakness, often accompanied by respiratory impairment or arthrogryposis. Weakness was predominantly proximal, with clinical courses that included deterioration, improvement, or stabilization. Three cases of King-Denborough syndrome were identified. Additional presentations included malignant hyperthermia and, in isolated cases, periodic paralysis. Muscle biopsies demonstrated considerable histologic heterogeneity, including fiber-size variation, internal nuclei, multiminicores, and fibrosis or dystrophic features. The pathogenic RYR1 variants included five compound-heterozygous genotypes, two homozygous variants, and two heterozygous variants. There was a positive correlation between variants located in the Bsol domain and disease severity. Conclusions: This cohort confirms and expands the clinical and histological diversity associated with RYR1 variants in Israel. Variants in the Bsol domain appear to be indicative of disease severity.
Heat stroke and the liver: mechanisms of injury and therapeutic strategies.
Global warming is leading to a continuous increase in the incidence of heat-related illnesses, among which heat stroke is the most severe type, characterized by a core body temperature > 40 °C and multiple organ dysfunction syndrome (MODS). The liver, being a thermosensitive organ, acts both as a target of injury and an "amplifier" of inflammation. Its acute injury and failure are significant causes of death in heat stress. This review summarizes the core mechanisms of heat stress-induced liver injury, including direct damage to hepatocytes by hyperthermia, the dual regulatory role of heat shock proteins (HSPs), gut barrier damage leading to endotoxemia and systemic inflammatory response, ischemia-reperfusion injury, and the involvement of various cell death modes such as apoptosis, pyroptosis, and ferroptosis. Clinically, liver injury manifests as a sharp rise in transaminases, abnormal bilirubin metabolism, and coagulation dysfunction, often combined with damage to the heart, brain, kidneys, and other organs, constituting MODS. Current treatments primarily focus on rapid cooling and organ support. Potential strategies include cell death inhibitors, antioxidants, and gut barrier protection. Severe cases may require artificial liver support systems (ALSS) or liver transplantation. Future efforts should delve deeper into the mechanisms of cell death, promote the clinical translation of targeted therapies, and strengthen effective prevention of heat stroke.
Heat stroke associated with novel leukaemia inhibitory factor receptor gene variant in a Chinese infant.
Stüve-Wiedemann syndrome (SWS) is a rare autosomal recessive genetic disorder characterised by skeletal dysplasia, dysautonomia, and multi-system abnormalities. It is typically caused by variants in the leukaemia inhibitory factor receptor (LIFR) gene. This case report presents a novel and complex heterozygous variant in the LIFR gene in a 2-month-old Chinese infant, which contributes to the limited literature on SWS in the Chinese population and underscores the importance of early identification and intervention. The infant was born at 38 weeks of gestation via caesarean section due to breech presentation. He presented with multiple symptoms, including persistent pulmonary hypertension of the newborn, recurrent hyperthermia, and joint deformities. Whole exome sequencing identified a novel compound heterozygous variant in the LIFR gene. The infant underwent various interventions, including mechanical ventilation, inhaled nitric oxide, and nasogastric feeding. Despite these measures, the infant experienced recurrent hyperthermia episodes leading to multi-organ dysfunction. The infant was eventually stabilised, but follow-up revealed global developmental delay and persistent skeletal abnormalities. Early identification of the LIFR gene variant is crucial for timely intervention and management of multi-system complications. Further research is warranted to explore targeted therapies and improve outcomes for patients with this rare disorder.
The Incidence of Volatile Anesthesia Porcine Stress Syndrome in Pigs (Sus scrofa domesticus) Gives Implications for Physiology during Anesthesia.
Pigs are extensively used for biomedical research as animal models given their similarities to humans including size, arterial capacity, and cutaneous structure. While their size also allows for the use of clinically available anesthesia equipment (for example, endotracheal tubes and ventilators), anecdotes exist with respect to stress reactions after exposure to volatile anesthetics. Over 3 mo at our institution, 11 pigs (Sus scrofa domesticus) exposed to isoflurane anesthesia during 2 research protocols were euthanized after exhibiting clinical signs of malignant hyperthermia, including hyperthermia, hypercapnia, skeletal muscle rigidity, dyspnea, tachycardia, and hypotension. This group was composed of intact Yorkshire/Landrace crosses (68 to 91 kg) purchased from a research breeder. While malignant hyperthermia is caused by a mutation in ryanodine receptor 1 (RYR1), another unnamed porcine stress syndrome is caused by a dystrophin defect. We analyzed the incidence of the RYR1 mutation and a dystrophin variant in 9 of the originally clinically affected pigs and in 56 subsequent pigs. All animals tested negative for the RYR1 mutation, while the dystrophin variant was found in 2 out of 7 clinical (28.6%) and 22 out of 46 (47.8%) subsequently tested female pigs. Creatine kinase, indicative of muscle damage, was slightly elevated at baseline in dystrophin variant-positive carriers, albeit not significantly. However, for the original clinically affected pigs, the increase in body temperature while under anesthesia was significantly greater in dystrophin variant-positive carriers (7.9 ± 0.8 °C) compared with noncarriers (5.2 ± 0.6 °C, P = 0.046). Taken together, we describe the suspected involvement of a dystrophin variant as one of the genetic etiologies in an unnamed condition that has been anecdotally experienced by pig researchers but not reported. We propose naming this condition volatile anesthesia porcine stress syndrome (VAPSS), which is an umbrella term that includes multiple genetic origins, the most well-known of which is malignant hyperthermia stress syndrome in pigs. Identifying other etiologies for VAPSS has implications for genetic and clinical screening to improve welfare in pigs bred for biomedical research and agricultural purposes.
When Parkinson's disease encounters high fever: two case reports and literature review.
Parkinson's disease (PD) is a chronic progressive neurodegenerative disorder. Acute hyperthermia syndrome (AHS) associated with PD is a critical neurological condition requiring immediate intervention. This article presents two cases of patients with PD with hyperthermia and provides a comprehensive comparative analysis across multiple dimensions, including etiology, pathogenesis, clinical features, diagnostic approaches, therapeutic strategies, and outcomes. The first patient exhibited motor dysfunction followed by hyperthermia, which was alleviated by adjusting the dosage of dopaminergic medication. In contrast, the second patient was initially misdiagnosed with sepsis, and his condition significantly improved with dopaminergic therapy. This report aimed to enhance clinicians' understanding of this syndrome, improve diagnostic precision, and facilitate the development of more effective treatment protocols for optimizing patient outcomes.
Publicações recentes
Ver todas no PubMed📚 EuropePMCmostrando 137
The Clinical, Histological, and Genetic Spectrum of RYR1 Variants-A Multi-Center Israeli Cohort Study.
Journal of clinical medicineHeat stroke and the liver: mechanisms of injury and therapeutic strategies.
European journal of medical researchWhen Parkinson's disease encounters high fever: two case reports and literature review.
American journal of translational researchHeat stroke associated with novel leukaemia inhibitory factor receptor gene variant in a Chinese infant.
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Annals of medicineDesflurane Safety Revisited: A Pharmacovigilance Study Detecting Potential Safety Signals from FAERS Data.
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CureusNovel heterozygous mutation in MYH3 causes contractures, pterygia, and spondylocarpostarsal fusion syndrome 1: A case report.
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EpilepsiaSudden Death Due To Excited Delirium Syndrome: From Pathophysiology To Postmortem Assessment: Case Reports.
La Clinica terapeuticaDiagnostic Value of Botryoid Nuclei as a Biomarker of Severe Hyperthermia and Systemic Inflammation in Heatstroke and Neuroleptic Malignant Syndrome: A Challenge of Climate Change.
International journal of laboratory hematologyThe evolving genetic landscape of neuromuscular fetal akinesias.
Journal of neuromuscular diseasesSingle-cell sequencing reveals the same heterogeneity of neutrophils in heatstroke-induced lung and liver injury.
Mucosal immunologyThe Incidence of Volatile Anesthesia Porcine Stress Syndrome in Pigs (Sus scrofa domesticus) Gives Implications for Physiology during Anesthesia.
Journal of the American Association for Laboratory Animal Science : JAALASStüve-Wiedemann syndrome with a novel variant in the LIFR gene: A case report.
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BMJ case reportsSerotonin Syndrome Induced by Fentanyl Alone in an Adult Patient After Cardiac Surgery: A Case Report.
CureusConcomitant Administration of Ozanimod and Serotonergic Antidepressants in Patients With Ulcerative Colitis or Relapsing Multiple Sclerosis.
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International medical case reports journalPhysiological role for S-nitrosylation of RyR1 in skeletal muscle function and development.
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International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia GroupA 4-Year-Old Boy with an Accidentally Detected Mutation in the RET Proto-Oncogene and Mutation in the Gene Encoding the Ryanodine Receptor1 (RyR1)-Case Report.
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HeliyonPaediatric survivors beyond infancy with Stüve-Wiedemann syndrome - A case series from the West Midlands, UK.
European journal of medical genetics[Analysis of a case of Multiple pterygium syndrome due to a novel variant of CHRNG gene].
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Annals of clinical and translational neurologyCombining Gene Mutation with Expression of Candidate Genes to Improve Diagnosis of Escobar Syndrome.
GenesSalmonella Enteritidis Fatal Septicemia with Meningoencephalitis in a Tiger (Panthera tigris) Cub.
Animals : an open access journal from MDPIHigh risk and low prevalence diseases: Serotonin syndrome.
The American journal of emergency medicineA case report and literature review: diagnosis and treatment of human immunodeficiency virus coinfected with visceral leishmania by metagenomic next-generation sequencing in China.
Annals of translational medicineLife-span characterization of epilepsy and comorbidities in Dravet syndrome mice carrying a targeted deletion of exon 1 of the Scn1a gene.
Experimental neurologyHeat stroke in dogs: Literature review.
Veterinarni medicinaHyperthermia and Serotonin: The Quest for a "Better Cyproheptadine".
International journal of molecular sciencesPostoperative hyperthermia-induced multiple organ failure in a child with Down syndrome: a case report.
Journal of medical case reportsNeuroleptic malignant-like syndrome associated multiple system atrophy: report on three cases.
BMC neurologyThermal dysregulation in patients with multiple sclerosis during SARS-CoV-2 infection. The potential therapeutic role of exercise.
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GenesThe endocannabinoid system impacts seizures in a mouse model of Dravet syndrome.
NeuropharmacologyEscitalopram, bupropion, lurasidone, lamotrigine and possible vortioxetine overdose presented with serotonin syndrome and diffuse encephalopathy: A case report.
Toxicology reportsParoxysmal hyperthermia, dysautonomia and rhabdomyolysis in a patient with Lesch-Nyhan syndrome.
JIMD reportsCase report: Spinal anesthesia for cesarean section in a parturient with Potocki-Lupski syndrome.
BMC anesthesiologyThe Clinical and Genotypic Spectrum of Scoliosis in Multiple Pterygium Syndrome: A Case Series on 12 Children.
GenesSuccessful Treatment of Severe Gamma-Hydroxybutyric Acid Withdrawal Syndrome With Dantrolene.
CureusCardiac anomalies associated with Escobar syndrome: A case report and a review of the literature.
MedicineCannabigerolic acid, a major biosynthetic precursor molecule in cannabis, exhibits divergent effects on seizures in mouse models of epilepsy.
British journal of pharmacologyDrugs of Abuse: Sympathomimetics.
Critical care clinicsDantrolene repurposed to treat sepsis or septic shock and COVID-19 patients.
European review for medical and pharmacological sciencesA systematic review of stereotactic radiofrequency ablation for hypothalamic hamartomas.
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Journal of veterinary emergency and critical care (San Antonio, Tex. : 2001)A Review of Genetic and Physiological Disease Mechanisms Associated With Cav1 Channels: Implications for Incomplete Congenital Stationary Night Blindness Treatment.
Frontiers in geneticsHomozygous intronic variants in TPM2 cause recessively inherited Escobar variant of multiple pterygium syndrome and congenital myopathy.
Neuromuscular disorders : NMDThe Role of α-Synuclein in Methamphetamine-Induced Neurotoxicity.
Neurotoxicity researchRyanodine receptor 1-related disorders: an historical perspective and proposal for a unified nomenclature.
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European review for medical and pharmacological sciencesTransdermal opioid patch in treatment of paroxysmal autonomic instability with dystonia with multiple cerebral insults: A case report.
MedicineAnesthesia for Stüve-Wiedemann syndrome: a rare adult patient case report.
Journal of applied geneticsRecessive MYH3 variants cause "Contractures, pterygia, and variable skeletal fusions syndrome 1B" mimicking Escobar variant multiple pterygium syndrome.
American journal of medical genetics. Part ASpinal anesthesia in a patient with Schwartz-Jampel syndrome.
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Minerva pediatricsUnderlying Serotonin Syndrome, Masked by Community-Acquired Pneumonia and Myocardial Ischemia.
The American journal of case reports[General anesthesia for Crisponi syndrome: case report].
Brazilian journal of anesthesiology (Elsevier)Focal and generalized seizure activity after local hippocampal or cortical ablation of NaV 1.1 channels in mice.
EpilepsiaA recurrent pathogenic variant in TPM2 reveals further phenotypic and genetic heterogeneity in multiple pterygium syndrome-related disorders.
Clinical geneticsAnesthesia Challenges in the Management of Freeman-Sheldon Syndrome: Report of Two Cases and Literature Review.
AANA journalInfusion of chimeric antigen receptor T cells against dual targets of CD19 and B-cell maturation antigen for the treatment of refractory multiple myeloma.
The Journal of international medical researchDravet syndrome as part of the clinical and genetic spectrum of sodium channel epilepsies and encephalopathies.
EpilepsiaComplications encountered in the treatment of primary and secondary hyperparathyroidism with microwave ablation - a retrospective study.
International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia GroupAdmission Body Temperature in Critically Ill Patients as an Independent Risk Predictor for Overall Outcome.
Medical principles and practice : international journal of the Kuwait University, Health Science Centre[Research progress in the heatstroke-induced myocardial injury].
Zhonghua wei zhong bing ji jiu yi xuePhenobarbital-induced anticonvulsant hypersensitivity syndrome in a cat.
The Journal of veterinary medical scienceCitalopram overdose and severe serotonin syndrome in an intermediate metabolizing patient.
The American journal of emergency medicineLethal multiple pterygium syndrome.
BMJ case reportsCHRNG-related nonlethal multiple pterygium syndrome: Muscle imaging pattern and clinical, histopathological, and molecular genetic findings.
American journal of medical genetics. Part AC57BL/6J and C57BL/6N substrains differentially influence phenotype severity in the Scn1a +/- mouse model of Dravet syndrome.
Epilepsia openMultiple Small Bowel Perforations Secondary to Tumor Lysis-a Complication of Pseudomyxoma Peritonei in a Patient Undergoing Intraperitoneal Chemotherapy.
Journal of gastrointestinal cancerLiver Transplantation for Fulminant Hepatic Failure Due to Heat Stroke: A Case Report.
Transplantation proceedingsEscobar Syndrome-An Multidisciplinary Approach for an Excellent Outcome With 3 Years of Follow-Up.
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial AssociationHomozygous/compound heterozygote RYR1 gene variants: Expanding the clinical spectrum.
American journal of medical genetics. Part ABladder wall and surrounding tissue necrosis following bilateral superselective embolization of internal iliac artery branches due to uncontrollable haematuria related to bladder tumor: case report.
CVIR endovascularLocal hyperthermia cleared multifarious viral warts in a patient with Cushing's syndrome.
Dermatologic therapyGrowth-Friendly Spine Surgery in Escobar Syndrome.
Journal of pediatric orthopedicsMolecular Diagnosis of Rare Autosomal Recessive Escobar Syndrome in a Consanguineous Pakistani Family.
Genetic testing and molecular biomarkersThermoregulation in epilepsy.
Handbook of clinical neurologyConsideration of Occult Infection and Sepsis Mimics in the Sick Patient Without an Apparent Infectious Source.
The Journal of emergency medicineOskar Kobyliński (1856-1926) and the first description of Noonan syndrome in the medical literature.
Journal of medical biographyMultiple, Independent T Cell Lymphomas Arising in an Experimentally FIV-Infected Cat during the Terminal Stage of Infection.
VirusesNon-pharmacological interventions for treating chronic prostatitis/chronic pelvic pain syndrome.
The Cochrane database of systematic reviewsRhabdomyolysis in Stuve-Wiedemann syndrome.
BMJ case reportsA successful anesthetic approach in a patient with Schwartz-Jampel syndrome.
Saudi journal of anaesthesiaPrenatal detection of uniparental disomy of chromosome 2 carrying a CHRND pathogenic variant that causes lethal multiple pterygium syndrome.
Clinical geneticsThe synthetic neuroactive steroid SGE-516 reduces seizure burden and improves survival in a Dravet syndrome mouse model.
Scientific reportsRetrospective evaluation of 155 adult equids and 21 foals with tetanus in Western, Northern, and Central Europe (2000-2014). Part 1: Description of history and clinical evolution.
Journal of veterinary emergency and critical care (San Antonio, Tex. : 2001)Hypothermia due to Antipsychotic Medication: A Systematic Review.
Frontiers in psychiatryComparative Assessment of the Heart's Functioning by Using the Akabane Test and Classical Methods of Instrumental Examination.
Journal of acupuncture and meridian studiesAnaesthetic management of a patient with multiple pterygium syndrome for elective caesarean section.
International journal of obstetric anesthesiaSerum histones as biomarkers of the severity of heatstroke in dogs.
Cell stress & chaperonesRisk factors for development of postoperative cerebellar mutism syndrome in children after medulloblastoma surgery.
Journal of neurosurgery. Pediatrics[Mutation analysis for a Chinese family affected with Escobar syndrome by whole exome sequencing].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical geneticsLethal multiple pterygium syndrome: A severe phenotype associated with a novel mutation in the nebulin gene.
Neuromuscular disorders : NMD[Surgical management of spinal deformity in a patient with Escobar syndrome: review of the literature].
Acta ortopedica mexicanaAnesthetic Outcomes of Children With Arthrogryposis Syndromes: No Evidence of Hyperthermia.
Anesthesia and analgesiaPharmacology and Toxicology of N-Benzylphenethylamine ("NBOMe") Hallucinogens.
Current topics in behavioral neurosciencesContinuous fetal head flexion as a marker for prenatal diagnosis of lethal multiple pterygium syndrome: a case report.
Journal of medical ultrasonics (2001)Intraoperative Presentation of Malignant Hyperthermia (Confirmed by RYR1 Gene Mutation, c.7522C>T; p.R2508C) Leads to Diagnosis of King-Denborough Syndrome in a Child With Hypotonia and Dysmorphic Features: A Case Report.
A & A case reportsEscobar (multiple pterygium) syndrome: Multidisciplinary approach to a very rare syndrome.
Eklem hastaliklari ve cerrahisi = Joint diseases & related surgeryFine Mapping of a Dravet Syndrome Modifier Locus on Mouse Chromosome 5 and Candidate Gene Analysis by RNA-Seq.
PLoS geneticsAnti-N-Methyl-D-Aspartate Receptor Encephalitis: A Potential Mimic of Neuroleptic Malignant Syndrome.
Pediatric neurologySurgical Approach, Findings, and Eight-Year Follow-Up in a Twenty-Nine Year Old Female With Freeman-Sheldon Syndrome Presenting With Blepharophimosis Causing Near-Complete Visual Obstruction.
The Journal of craniofacial surgeryChallenges in a large mixed drug overdose patient.
BMJ case reportsβ1-C121W Is Down But Not Out: Epilepsy-Associated Scn1b-C121W Results in a Deleterious Gain-of-Function.
The Journal of neuroscience : the official journal of the Society for NeuroscienceTreatment of Dravet Syndrome.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiquesTruncating CHRNG mutations associated with interfamilial variability of the severity of the Escobar variant of multiple pterygium syndrome.
BMC geneticsPerioperative Diagnosis and Treatment of Serotonin Syndrome Following Administration of Methylene Blue.
The American journal of case reportsA Case of Freeman-Sheldon Syndrome: Anesthetic Challenges.
Journal of the Mississippi State Medical AssociationLethal multiple pterygium syndrome, the extreme end of the RYR1 spectrum.
BMC musculoskeletal disordersCardiorespiratory control and cytokine profile in response to heat stress, hypoxia, and lipopolysaccharide (LPS) exposure during early neonatal period.
Physiological reports[Fatal hyperpyrexia in an adolescent patient with severe burns after a traffic accident].
Der UnfallchirurgA case of malignant hyperthermia that was difficult to be differentiated from oral antipsychotic polypharmacy-associated neuroleptic malignant syndrome.
JA clinical reportsBilateral congenital lumbar hernias in a patient with central core disease--A case report.
Neuromuscular disorders : NMDSudden Cardiac Death and Post Cardiac Arrest Syndrome. An Overview.
Journal of critical care medicine (Universitatea de Medicina si Farmacie din Targu-Mures)Methamphetamine oxidative stress, neurotoxicity, and functional deficits are modulated by nuclear factor-E2-related factor 2.
Free radical biology & medicinePreliminary experience with delayed non-operative therapy of multiple hand and wrist contractures in a woman with Freeman-Sheldon syndrome, at ages 24 and 28 years.
BMJ case reportsStüve-Wiedemann syndrome in a neonate.
Pediatrics international : official journal of the Japan Pediatric SocietyAnimal models for mesiotemporal lobe epilepsy: The end of a misunderstanding?
Revue neurologiqueAssociações
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Referências e fontes
Bases de dados externas citadas neste artigo
Publicações científicas
Artigos indexados no PubMed ligados a esta doença no grafo RarasNet — título, periódico e PMID direto da fonte, sem intermediação de IA.
- The Clinical, Histological, and Genetic Spectrum of RYR1 Variants-A Multi-Center Israeli Cohort Study.
- Heat stroke and the liver: mechanisms of injury and therapeutic strategies.
- Heat stroke associated with novel leukaemia inhibitory factor receptor gene variant in a Chinese infant.
- The Incidence of Volatile Anesthesia Porcine Stress Syndrome in Pigs (Sus scrofa domesticus) Gives Implications for Physiology during Anesthesia.Journal of the American Association for Laboratory Animal Science : JAALAS· 2025· PMID 40035276mais citado
- When Parkinson's disease encounters high fever: two case reports and literature review.
- Pregnancy in GNE myopathy patients: a nationwide repository survey in Japan.
Bases de dados e fontes oficiais
Identificadores e referências canônicas usadas para montar este verbete.
- ORPHA:2215(Orphanet)
- OMIM OMIM:217150(OMIM)
- MONDO:0009012(MONDO)
- GARD:3361(GARD (NIH))
- Busca completa no PubMed(PubMed)
- Q55781764(Wikidata)
Dados compilados pelo RarasNet a partir de fontes abertas (Orphanet, OMIM, MONDO, PubMed/EuropePMC, ClinicalTrials.gov, DATASUS, PCDT/MS). Este conteúdo é informativo e não substitui avaliação médica.
Conteúdo mantido por Agente Raras · Médicos e pesquisadores podem colaborar