A síndrome de Morvan é uma doença neurológica adquirida rara, com risco de vida, caracterizada por neuromiotonia, disautonomia e encefalopatia com insônia grave. Sinais envolvendo hiperatividade central (por exemplo, alucinações, confusão, amnésia, mioclonia), autonômica (por exemplo, variações na pressão arterial, hiperidrose) e periférica (por exemplo, cólicas dolorosas, mioquimia), bem como manifestações sistêmicas (como perda de peso, prurido, febre). O timoma está presente em alguns casos.
Introdução
O que você precisa saber de cara
A síndrome de Morvan é uma doença neurológica adquirida rara, com risco de vida, caracterizada por neuromiotonia, disautonomia e encefalopatia com insônia grave. Sinais envolvendo hiperatividade central (por exemplo, alucinações, confusão, amnésia, mioclonia), autonômica (por exemplo, variações na pressão arterial, hiperidrose) e periférica (por exemplo, cólicas dolorosas, mioquimia), bem como manifestações sistêmicas (como perda de peso, prurido, febre). O timoma está presente em alguns casos.
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
Características mais comuns
Os sintomas variam de pessoa para pessoa. Abaixo estão as 1 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 Morvan
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Pesquisa ativa
Ensaios clínicos abertos e novidades científicas recentes
Pesquisa e ensaios clínicos
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Publicações mais relevantes
Morvan syndrome in a patient with progressing metastatic thymoma and myasthenia gravis.
Morvan syndrome (MoS) is a rare paraneoplastic syndrome that is predominantly characterised by autonomic dysfunction, peripheral nerve hyperexcitability and altered mental status. Cases in literature often describe pre-existing autoimmune diagnoses in patients with MoS, alluding to its association with systemic immune dysregulation.We report a woman presenting with hypersomnolence and fluctuating mental status consistent with MoS who had been previously diagnosed with metastatic thymoma, acetylcholine receptor-positive myasthenia gravis and multiple other chronic medical conditions. The report emphasises the importance of prompt recognition of symptoms and accurate diagnosis in rare diseases, allowing for timely initiation of the appropriate immunotherapy that ultimately led to rapid and significant clinical improvement.
CASPR2 antibody-related neurological syndromes in children: three cases report and literature review.
Contactin-associated protein-like 2 (CASPR2) antibody-related neurological syndrome is well defined in adults, while data in children is rare. We perform this case series and literature review to ascertain the clinical features of this disorder in children. We describe three cases who were diagnosed with CASPR2 antibody-related neurological syndrome, and then systematically characterized clinical features, therapeutic responses, and outcomes in 64 patients in literature. Among the 67 patients, the median age was 8.4 years (range 0.5–18), with a male predominance (65.7%). The most characteristic symptoms of CASPR2 antibody-related neurological syndrome include psychiatric abnormalities (68.7%), sleep disorders (55.2%), dysautonomia (44.8%), movement disorders (43.3%), seizures (41.8%), neuropathic pain (34.3%), and cognitive disturbances (31.3%). Autoimmune encephalitis (AE, 62.7%) was most frequent, followed by Morvan syndrome (MoS, 26.9%) and peripheral nerve hyperexcitability (PNH, 7.5%). CASPR2 antibodies are typically detected in serum (85.1%), but rarely in CSF exclusively (3.0%). Investigations revealed abnormalities in CSF analysis (22.9%; 13 AE, 5 MoS), brain MRI (24.1%; 11 AE, 3 MoS), and EEG (67.3%; 26 AE, 7 MoS). Neoplasm was not found in our case series and literature review. Regarding treatment, 46 patients received first-line immunotherapy alone, while 5 required second-line treatment. Immunotherapy demonstrated highly effective, with 95.8% achieving a favorable outcome (mRS score ≤ 2) and a low recurrence rate of 5.1%. We therefore recommend that all children presenting with new-onset psychiatric abnormalities, sleep disorders, dysautonomia, movement disorders, seizures, neuropathic pain, and cognitive disturbances should be suspected of having CASPR2 antibody-related neurological syndrome. Neoplastic processes are rare in pediatric patients. Early recognition of the disease is important because it responds well to immunotherapy. The online version contains supplementary material available at 10.1186/s12887-026-06549-4.
Morvan Syndrome Masquerading as Anxiety Disorder: A Case Report Highlighting the Importance of Recognizing Organic Signs in Psychiatric Settings.
Morvan syndrome is a rare subtype of autoimmune encephalitis, primarily characterized by increased peripheral nerve excitability, autonomic dysfunction, and severe insomnia. This report presents a 28-year-old female patient who sought medical attention due to widespread pain, refractory insomnia, limb sensory abnormalities, and low mood, initially diagnosed as "anxiety disorder". Neurological examination revealed muscle twitching in the limbs. Electromyography indicated increased peripheral nerve excitability, with serum testing showing weak positivity for anti-Leucine-rich Glioma Inactivated 1 (LGI-1) IgG antibodies and strong positivity for anti-Contactin-associated Protein-like 2 (CASPR2) IgG antibodies. Cerebrospinal fluid Pandy's test was weakly positive. The final diagnosis was Morvan syndrome complicated by anxiety disorder. Following treatment, the patient's symptoms significantly improved. This case highlights the diagnostic challenges of Morvan syndrome, particularly when patients present with prominent psychiatric symptoms that mimic functional disorders. It underscores the critical importance of screening for subtle organic signs-specifically fasciculations and widespread pain-in patients with refractory anxiety to prevent misdiagnosis and facilitate timely immunotherapy.
Morvan syndrome associated with prominent Tau pathology: A clinicopathological case report.
We report a case of Morvan syndrome in a 48-year-old man, emphasizing the presence of prominent tau pathology in the frontal cortex identified during postmortem examination. Morvan syndrome is characterized by peripheral nerve hyperexcitability, autonomic dysfunction, and encephalopathy, and is often associated with antibodies against LGI1 and Caspr2. Clinical assessment documented neurological, autonomic, and cognitive symptoms consistent with Morvan syndrome. Serological testing confirmed LGI1 and Caspr2 antibodies. Despite treatment, the patient suffered fatal cardiac arrest. Full autopsy, including detailed neuropathological assessment, was performed, with specific examination of neuronal and glial tau pathology. Autopsy revealed a thymoma and extensive tau accumulation in the frontal cortex with neuronal and astrocytic involvement. Neurofibrillary tangles, pretangles, and astroglial tau aggregates were detected. The patient had no history of repetitive head trauma or participation in contact sports. This case suggests a potential association between immune-mediated disorders-specifically Morvan syndrome with LGI1 and Caspr2 antibodies-and focal tau pathology. The coexistence of autoimmune features and tau deposition raises questions about shared or interacting pathophysiological mechanisms. Further research is warranted to clarify these relationships.
A rare presentation of CASPR2-associated Morvan syndrome overlapping with GM1-positive AMSAN: a case report.
Morvan syndrome is a rare autoimmune disorder characterized by peripheral nerve hyperexcitability with autonomic and central nervous system involvement, most commonly associated with antibodies against contactin-associated protein-like 2 (CASPR2). Acute motor and sensory axonal neuropathy (AMSAN) is an axonal variant of Guillain-Barré syndrome linked to anti-ganglioside antibodies and often manifests as severe limb weakness. Their concurrent presentation is unusual and raises the possibility of shared immune targets within peripheral nerve microdomains. A 70-year-old man presented with a relapsing course of progressive lower-limb weakness accompanied by widespread muscle twitching, severe insomnia with nocturnal hyperarousal, and refractory constipation. He had a prior episode diagnosed as AMSAN that improved after immunotherapy but relapsed four months after treatment was discontinued. Neurological examination demonstrated bilateral lower-limb weakness with reduced tendon reflexes. Moreover, electrophysiological studies confirmed diffuse multifocal peripheral nerve injury with superimposed peripheral nerve hyperexcitability. In addition, immunologic testing revealed serum anti-GM1 antibodies and anti-CASPR2 IgG in both serum and cerebrospinal fluid. Collectively, these findings supported a diagnosis of recurrent AMSAN coexisting with CASPR2-associated Morvan syndrome. Combined immunotherapy with corticosteroids and intravenous immunoglobulin, alongside symptomatic management, resulted in marked clinical improvement. This case report describes a rare overlap of relapsing AMSAN and Morvan syndrome. This antibody-defined coexistence is hypothesis-generating and may reflect synergistic immune injury involving nodal and paranodal regions. This case underscores the importance of recognizing overlapping phenotypes to guide diagnostic profiling and immunomodulatory therapy.
Publicações recentes
Morvan syndrome in a patient with progressing metastatic thymoma and myasthenia gravis.
Morvan Syndrome Masquerading as Anxiety Disorder: A Case Report Highlighting the Importance of Recognizing Organic Signs in Psychiatric Settings.
Morvan syndrome associated with prominent Tau pathology: A clinicopathological case report.
A rare presentation of CASPR2-associated Morvan syndrome overlapping with GM1-positive AMSAN: a case report.
A Rare Adolescent Presentation of Morvan Syndrome: Diagnostic Challenges and Therapeutic Response.
📚 EuropePMC71 artigos no totalmostrando 111
Morvan syndrome in a patient with progressing metastatic thymoma and myasthenia gravis.
BMJ case reportsMorvan Syndrome Masquerading as Anxiety Disorder: A Case Report Highlighting the Importance of Recognizing Organic Signs in Psychiatric Settings.
International medical case reports journalMorvan syndrome associated with prominent Tau pathology: A clinicopathological case report.
Journal of neuroimmunologyA rare presentation of CASPR2-associated Morvan syndrome overlapping with GM1-positive AMSAN: a case report.
Frontiers in immunologyA Rare Adolescent Presentation of Morvan Syndrome: Diagnostic Challenges and Therapeutic Response.
Clinical case reportsCASPR2 antibody-related neurological syndromes in children: three cases report and literature review.
BMC pediatricsVideo-Polysomnography in Peripheral Nerve Hyperexcitability: Clues to Morvan Syndrome in Two Patients and Literature Review.
Journal of clinical neurophysiology : official publication of the American Electroencephalographic SocietyThymectomy for Morvan Syndrome Associated With Thymoma.
Annals of thoracic surgery short reportsA Rare Case Report of Morvan Syndrome: A Constellation of Autonomic, Central and Peripheral Nervous System Involvement.
CureusGlutamic Acid Decarboxylase Antibody Unexpectedly Detected During Recovery Phase in Three Patients With Voltage-Gated Potassium Channel Antibody-Related Autoimmune Encephalitis.
CureusDual diagnosis at the neuro-immune interface: a case report of neuronal intranuclear inclusion disease with acute anti-CASPR2 encephalitis.
Frontiers in immunologyNeuropathic pain in CASPR2 antibody disease spectrum: A systematic review.
Journal of neuroimmunologyMorvan syndrome with bilateral basal ganglia hyperintensities and exfoliative skin rashes in a patient with Chronic Hepatitis B: A diagnostic and therapeutic dilemma.
Clinical neurology and neurosurgeryAnesthetic Management of a Patient with Morvan Syndrome.
Journal of cardiothoracic and vascular anesthesiaElectroencephalography and polysomnography as predictors of long-term functional outcomes in anti-CASPR2 encephalitis: A multicenter cohort study.
Epileptic disorders : international epilepsy journal with videotapeAutoimmune encephalitis with CASPR2 antibody: A case series and updated literature review.
International immunopharmacologyUnmasking Anti-CASPR2 Syndrome in a Patient Treated for Myasthenia Gravis in the Era of New Treatments.
European journal of neurologyExploring Telitacicept for Neurological Autoimmune Disorders: A Case Study on Morvan Syndrome.
The American journal of case reportsSuccessful treatment of morvan syndrome with efgartigimod: report of two cases.
Journal of neurologyLeucine-rich glioma-inactivated protein 1 antibody-positive limbic encephalitis in a patient with an early-stage asymptomatic breast cancer.
BMJ case reportsA case series: Three cases of Morvan's syndrome as a rare autoimmune disorder with anti-Caspr2 antibody.
MedicineA Case Report of an Atypical Presentation of Morvan Syndrome.
CureusA rare case of LGI1 antibody-positive Morvan syndrome with myasthenia gravis.
Medicina clinicaThe neurobiology and immunology of CASPR2-associated neurological disorders.
Revue neurologiqueCharacteristics of after-discharges following compound muscle action potential or F-wave in primary peripheral nerve hyperexcitability syndrome.
Muscle & nerveMorvan Fibrillary Chorea Associated with Monoclonal B Cell Lymphocytosis.
The American journal of case reportsAnesthetic Management of Patients With Morvan Syndrome: A Case Report and Literature Review.
CureusParaneoplastic autoimmune neurologic disorders associated with thymoma.
Handbook of clinical neurologyMorvan Syndrome Associated With Anti-LGI1 Antibodies and Thymoma.
Journal of clinical neurology (Seoul, Korea)Autonomic nervous system involvement in autoimmune encephalitis and paraneoplastic neurological syndromes.
Revue neurologiqueOccult bowel cancer presenting as Morvan syndrome.
BMJ case reportsDistinct phenotypes in a cohort of anti-CASPR2 associated neurological syndromes.
Clinical neurology and neurosurgeryMotor symptoms in nonparaneoplastic CNS disorders associated with neural antibodies.
Handbook of clinical neurologyAnesthetic management of patients with Morvan syndrome - A rare disorder.
Saudi journal of anaesthesiaClinical features of 28 cases of anti-leucine-rich glioma-inactivated protein 1 encephalitis and anti-contactin-associated protein-like 2 encephalitis.
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciencesContactin-Associated Protein-Like 2-Related Peripheral Nerve Hyperexcitability Associated With Charcot-Marie-Tooth Type 4F.
The NeurohospitalistMorvan's syndrome: An unusual presentation of a solid pseudopapillary pancreatic tumor.
Journal of neurosciences in rural practiceA Case of Anti-Caspr2 Autoimmune Encephalitis Associated with Adenocarcinoma of the Lung.
European journal of case reports in internal medicineAutoimmune neuromyotonia.
Current opinion in neurologyMorvan Syndrome Manifesting as Autoimmune Paraneoplastic Encephalitis Associated with Thymoma and Antivoltage Gated Potassium Channel (Leucine Rich, Glioma Inactivated 1) Antibody Detected using F 18 Fluorodeoxyglucose Positron Emission Tomography/Computed Tomography.
Indian journal of nuclear medicine : IJNM : the official journal of the Society of Nuclear Medicine, India[Morvan syndrome associated with unresectable thymoma responsive to chemotherapy: a case report].
Rinsho shinkeigaku = Clinical neurologyGuillain-Barré-like syndrome: an uncommon feature of CASPR2 and LGI1 autoimmunity.
Journal of neurologyRefractory Morvan syndrome responsive to rituximab: a case report and review of the literature.
Neuromuscular disorders : NMDSleep Disorders and Autoimmunity: Insomnia as the Presenting Sign of Morvan Syndrome Associated with CASPR2 Antibodies.
Noro psikiyatri arsivi[Morvan syndrome with positive anti LGI1/CASPR2 antibodies in serum/cerebrospinal fluid:a case report and literature review].
Zhonghua nei ke za zhiPhenotypic Spectrum of CASPR2 and LGI1 Antibodies Associated Neurological Disorders in Children.
Frontiers in pediatricsBilateral Panuveitis Associated with Morvan Syndrome: A Case Report and Review of the Literature.
Ocular immunology and inflammationAutoimmune Neurological Disorders with IgG4 Antibodies: a Distinct Disease Spectrum with Unique IgG4 Functions Responding to Anti-B Cell Therapies.
Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeuticsExtrapleural pneumonectomy for recurrent thymoma diagnosed after return of paraneoplastic Morvan syndrome.
Journal of surgical case reportsObjective sleep profile in LGI1/CASPR2 autoimmunity.
SleepIgG4-Mediated Neurologic Autoimmunities: Understanding the Pathogenicity of IgG4, Ineffectiveness of IVIg, and Long-Lasting Benefits of Anti-B Cell Therapies.
Neurology(R) neuroimmunology & neuroinflammationMorvan Syndrome Converted from Isaacs' Syndrome after Thymectomy with Positivity for Both Anti-LGI1 and Anti-CASPR2 Antibodies.
Internal medicine (Tokyo, Japan)Electrodiagnostic Assessment of Hyperexcitable Nerve Disorders.
Neurologic clinicsCASPR2-Related Morvan Syndrome: Autonomic, Polysomnographic, and Neuropsychological Observations.
Neurology. Clinical practiceA case report of Morvan syndrome.
Oxford medical case reportsClinical Profile and Treatment Response in Patients with CASPR2 Antibody-Associated Neurological Disease.
Annals of Indian Academy of NeurologyDemystifying the spontaneous phenomena of motor hyperexcitability.
Clinical neurophysiology : official journal of the International Federation of Clinical NeurophysiologyClinical Character of CASPR2 Autoimmune Encephalitis: A Multiple Center Retrospective Study.
Frontiers in immunologyPediatric LGI1 and CASPR2 autoimmunity associated with COVID 19: Morvan syndrome.
Journal of neurologyMorvan syndrome associated with LGI1 antibody: a case report.
BMC neurologyTotal Wake: Natural, Pathological, and Experimental Limits to Sleep Reduction.
Frontiers in neuroscienceSleep Disturbances Associated with Neurological Autoimmunity.
Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeuticsAnesthetic Management of Robotic Thymectomy in a Patient With Morvan Syndrome: A Case Report.
A&A practiceCaspr2 autoantibody-associated Morvan syndrome predating thymoma relapse by 30 months.
Lung cancer (Amsterdam, Netherlands)Morvan syndrome: case report.
Medicina clinicaClinical characteristics of patients double positive for CASPR2 and LGI1-antibodies.
Clinical neurology and neurosurgeryAnti-CASPR2 clinical phenotypes correlate with HLA and immunological features.
Journal of neurology, neurosurgery, and psychiatryCASPR2 autoimmunity in children expanding to mild encephalopathy with hypertension.
NeurologyExpanding clinical spectrum of Caspr2 antibody-associated disease: warning on brainstem involvement and respiratory failure.
Journal of the neurological sciencesMorvan Syndrome and Diffuse Large B-Cell Lymphoma in the Central Nervous System.
The neurologistMercury-induced autoimmunity: Report of two adolescent siblings with Morvan syndrome "plus" and review of the literature.
Journal of neuroimmunologySystematic review of the clinical spectrum of CASPR2 antibody syndrome.
Journal of neurologyInsomnia and Dysautonomia with Contactin-Associated Protein 2 and Leucine-Rich Glioma Inactivated Protein 1 Antibodies: A "Forme Fruste" of Morvan Syndrome?
Case reports in neurology[Ectopic Hilar Thymoma Associated with Morvan Syndrome after Extended Thymectomy for Myasthenia Gravis].
Kyobu geka. The Japanese journal of thoracic surgerySuccessful therapeutic plasma exchange in a patient with Morvan syndrome.
Asian journal of transfusion scienceLGI1 and CASPR2 autoimmunity in children: Systematic literature review and report of a young girl with Morvan syndrome.
Journal of neuroimmunologyClinical characteristics of autoimmune disorders in the central nervous system associated with myasthenia gravis.
Journal of neurologyPeripheral nerve hyperexcitability.
Handbook of clinical neurologyFatal familial insomnia and Agrypnia Excitata: Autonomic dysfunctions and pathophysiological implications.
Autonomic neuroscience : basic & clinicalDelayed onset of severe chronic pain in CASPR2 autoantibody-associated Morvan syndrome in a former UK swine abattoir worker.
Pain reportsAdmission diagnoses of patients later diagnosed with autoimmune encephalitis.
Journal of neurologyUpdates in the Diagnosis and Treatment of Paraneoplastic Neurologic Syndromes.
Current oncology reportsAssociation of Leucine-Rich Glioma Inactivated Protein 1, Contactin-Associated Protein 2, and Contactin 2 Antibodies With Clinical Features and Patient-Reported Pain in Acquired Neuromyotonia.
JAMA neurologyMichel Jouvet as a clinical neurophysiologist and neurologist.
Sleep medicineA Phase II Study of Pemetrexed in Patients with Recurrent Thymoma and Thymic Carcinoma.
Journal of thoracic oncology : official publication of the International Association for the Study of Lung CancerMorvan syndrome associated with CASPR2 and LGI1 antibodies in a child.
NeurologyFunctional Impairments in a Patient with Morvan Syndrome: A Case Presentation.
PM & R : the journal of injury, function, and rehabilitationPeripheral Nerve Hyperexcitability Syndromes.
Continuum (Minneapolis, Minn.)Morvan syndrome: a rare cause of syndrome of inappropriate antidiuretic hormone secretion.
Clujul medical (1957)Autoimmune episodic ataxia in patients with anti-CASPR2 antibody-associated encephalitis.
Neurology(R) neuroimmunology & neuroinflammationMorvan syndrome as a paraneoplastic disorder of thymoma with anti-CASPR2 antibodies.
Lancet (London, England)Netrin-1 receptor antibodies in thymoma-associated neuromyotonia with myasthenia gravis.
NeurologyFatal Morvan Syndrome Associated With Myasthenia Gravis.
The neurologistClinical utility of seropositive voltage-gated potassium channel-complex antibody.
Neurology. Clinical practiceMorvan syndrome with Caspr2 antibodies. Clinical and autopsy report.
Journal of the neurological sciencesAnti-contactin-associated protein-2 encephalitis: relevance of antibody titres, presentation and outcome.
European journal of neurologyEncephalopathy with upper body hypertonia and myoclonus in patient with systemic lupus erythematosus and anti-CASPR2.
LupusCharacterization of a Subtype of Autoimmune Encephalitis With Anti-Contactin-Associated Protein-like 2 Antibodies in the Cerebrospinal Fluid, Prominent Limbic Symptoms, and Seizures.
JAMA neurologyThe clinical spectrum of Caspr2 antibody-associated disease.
NeurologyMorvan Syndrome Secondary to Thymic Carcinoma in a Patient with Systemic Lupus Erythematosus.
Case reports in neurological medicineA Case of Morvan Syndrome Mimicking Amyotrophic Lateral Sclerosis With Frontotemporal Dementia.
Journal of clinical neuromuscular diseaseAutoimmune sleep disorders.
Handbook of clinical neurologyA Chinese female Morvan patient with LGI1 and CASPR2 antibodies: a case report.
BMC neurologyA Case Series of Patients With Autoimmune Myasthenia Gravis in Association With Invasive Thymoma.
Journal of clinical neuromuscular diseaseMorvan Syndrome: A Case Report With Patient Narrative and Video.
The Neurohospitalist[Intravenous immunoglobulin therapy in Morvan syndrome secondary to recurrent thymic carcinoma].
MedwaveThymoma associated with autoimmune diseases: 85 cases and literature review.
Autoimmunity reviewsPeripheral small fiber dysfunction and neuropathic pain in patients with Morvan syndrome.
NeurologyInhibitory axons are targeted in hippocampal cell culture by anti-Caspr2 autoantibodies associated with limbic encephalitis.
Frontiers in cellular neuroscienceStatus dissociatus and disturbed dreaming in a patient with Morvan syndrome plus myasthenia gravis.
Sleep medicineImmunotherapy of oneiric stupor in Morvan syndrome: Efficacy documented by actigraphy.
NeurologyAssociações
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Comunidades
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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.
- Morvan syndrome in a patient with progressing metastatic thymoma and myasthenia gravis.
- CASPR2 antibody-related neurological syndromes in children: three cases report and literature review.
- Morvan Syndrome Masquerading as Anxiety Disorder: A Case Report Highlighting the Importance of Recognizing Organic Signs in Psychiatric Settings.
- Morvan syndrome associated with prominent Tau pathology: A clinicopathological case report.
- A rare presentation of CASPR2-associated Morvan syndrome overlapping with GM1-positive AMSAN: a case report.
- A Rare Adolescent Presentation of Morvan Syndrome: Diagnostic Challenges and Therapeutic Response.
Bases de dados e fontes oficiais
Identificadores e referências canônicas usadas para montar este verbete.
- ORPHA:83467(Orphanet)
- MONDO:0008718(MONDO)
- GARD:9766(GARD (NIH))
- Busca completa no PubMed(PubMed)
- Artigo Wikipedia(Wikipedia)
- Q2964544(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
