Raras
Buscar doenças, sintomas, genes...
Cefaleia hípica
ORPHA:276429CID-10 · G44.8CID-11 · 8A83DOENÇA RARA

Condições nas quais o sintoma principal é dor de cabeça e a dor de cabeça não podem ser atribuídas a nenhuma causa conhecida.

Mantido por Agente Raras·Colaborar como especialista →

Introdução

O que você precisa saber de cara

📋

Condições nas quais o sintoma principal é dor de cabeça e a dor de cabeça não podem ser atribuídas a nenhuma causa conhecida.

Publicações científicas
186 artigos
Último publicado: 2026 Jan 28
Medicamentos
7 registrados
ACETAMINOPHEN, CAFFEINE, ZOLMITRIPTAN

Tem tratamento?

7 medicamentos registrados
Ver detalhes, fases e interações →
ACETAMINOPHENCAFFEINEZOLMITRIPTANDIHYDROERGOTAMINE MESYLATEALMOTRIPTAN MALATENARATRIPTAN HYDROCHLORIDEDICLOFENAC POTASSIUM

Escala de raridade

CLASSIFICAÇÃO ORPHANET · BRASIL 2024
Unknown
Ultra-rara
<1/50k
Muito rara
1/20k
Rara
1/10k
Pouco freq.
1/5k
Incomum
1/2k
Prevalência
0.0
Worldwide
Início
Adult
+ childhood, elderly
🏥
SUS: Cobertura mínimaScore: 15%
CID-10: G44.8
🇧🇷Dados SUS / DATASUS
PROCEDIMENTOS SIGTAP (2)
0202010694
Sequenciamento completo do exoma (WES)genetic_test
0301070040
Atendimento em reabilitação — doenças rarasrehabilitation
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Entender a doença

Do básico ao detalhe, leia no seu ritmo

Preparando trilha educativa...

Sinais e sintomas

O que aparece no corpo e com que frequência cada sintoma acontece

Partes do corpo afetadas

🧠
Neurológico
20 sintomas
👁️
Olhos
9 sintomas
😀
Face
5 sintomas
👂
Ouvidos
5 sintomas
🫃
Digestivo
3 sintomas
💪
Músculos
3 sintomas

+ 58 sintomas em outras categorias

Características mais comuns

Parestesia
Sensação de dor espontânea
Diabetes mellitus
Fotofobia
Instabilidade postural
Pleocitose linfocitária do LCR
106sintomas
Sem dados (106)

Os sintomas variam de pessoa para pessoa. Abaixo estão as 106 características clínicas mais associadas, ordenadas por frequência.

ParestesiaParesthesia
Sensação de dor espontâneaSpontaneous pain sensation
Diabetes mellitus
FotofobiaPhotophobia
Instabilidade posturalPostural instability

Linha do tempo da pesquisa

Publicações por ano — veja quando o interesse científico cresceu
Anos de pesquisa1desde 2026
Total histórico186PubMed
Últimos 10 anos50publicações
Pico20197 papers
Linha do tempo
2026Hoje · 2026📈 2019Ano de pico
Publicações por ano (últimos 10 anos)

Encontrou um erro ou informação desatualizada? Sugira uma correção →

Genética e causas

O que está alterado no DNA e como passa nas famílias

Genes associados

4 genes identificados com associação a esta condição. Padrão de herança: Not applicable.

CACNA1AVoltage-dependent P/Q-type calcium channel subunit alpha-1ADisease-causing germline mutation(s) inAltamente restrito
FUNÇÃO

Voltage-sensitive calcium channels (VSCC) mediate the entry of calcium ions into excitable cells and are also involved in a variety of calcium-dependent processes, including muscle contraction, hormone or neurotransmitter release, gene expression, cell motility, cell division and cell death. The isoform alpha-1A gives rise to P and/or Q-type calcium currents. P/Q-type calcium channels belong to the 'high-voltage activated' (HVA) group and are specifically blocked by the spider omega-agatoxin-IVA

LOCALIZAÇÃO

Cell membrane

VIAS BIOLÓGICAS (2)
Presynaptic depolarization and calcium channel openingRegulation of insulin secretion
MECANISMO DE DOENÇA

Spinocerebellar ataxia 6

Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA6 is an autosomal dominant cerebellar ataxia (ADCA), mainly caused by expansion of a CAG repeat in the coding region of CACNA1A. There seems to be a correlation between the repeat number and earlier onset of the disorder.

OUTRAS DOENÇAS (9)
migraine, familial hemiplegic, 1episodic ataxia type 2developmental and epileptic encephalopathy, 42spinocerebellar ataxia type 6
HGNC:1388UniProt:O00555
PRRT2Proline-rich transmembrane protein 2Candidate gene tested inRestrito
FUNÇÃO

As a component of the outer core of AMPAR complex, may be involved in synaptic transmission in the central nervous system. In hippocampal neurons, in presynaptic terminals, plays an important role in the final steps of neurotransmitter release, possibly by regulating Ca(2+)-sensing. In the cerebellum, may inhibit SNARE complex formation and down-regulate short-term facilitation

LOCALIZAÇÃO

Cell membranePresynaptic cell membraneSynapseCell projection, axonCytoplasmic vesicle, secretory vesicle, synaptic vesicle membranePostsynaptic density membraneCell projection, dendritic spine

MECANISMO DE DOENÇA

Episodic kinesigenic dyskinesia 1

An autosomal dominant form of paroxysmal kinesigenic dyskinesia, a neurologic condition characterized by recurrent and brief attacks of abnormal involuntary movements, triggered by sudden voluntary movement. These attacks usually have onset during childhood or early adulthood and can involve dystonic postures, chorea, or athetosis.

EXPRESSÃO TECIDUAL(Ubíquo)
Cerebelo
606.4 TPM
Cérebro - Hemisfério cerebelar
563.4 TPM
Ovário
183.2 TPM
Brain Frontal Cortex BA9
167.2 TPM
Córtex cerebral
152.5 TPM
OUTRAS DOENÇAS (9)
episodic kinesigenic dyskinesia 1seizures, benign familial infantile, 2infantile convulsions and choreoathetosisfamilial or sporadic hemiplegic migraine
HGNC:30500UniProt:Q7Z6L0
SCN1ASodium channel protein type 1 subunit alphaDisease-causing germline mutation(s) inAltamente restrito
FUNÇÃO

Pore-forming subunit of Nav1.1, a voltage-gated sodium (Nav) channel that directly mediates the depolarizing phase of action potentials in excitable membranes. Navs, also called VGSCs (voltage-gated sodium channels) or VDSCs (voltage-dependent sodium channels), operate by switching between closed and open conformations depending on the voltage difference across the membrane. In the open conformation they allow Na(+) ions to selectively pass through the pore, along their electrochemical gradient.

LOCALIZAÇÃO

Cell membrane

VIAS BIOLÓGICAS (2)
Interaction between L1 and AnkyrinsPhase 0 - rapid depolarisation
MECANISMO DE DOENÇA

Generalized epilepsy with febrile seizures plus 2

A rare autosomal dominant, familial condition with incomplete penetrance and large intrafamilial variability. Patients display febrile seizures persisting sometimes beyond the age of 6 years and/or a variety of afebrile seizure types. This disease combines febrile seizures, generalized seizures often precipitated by fever at age 6 years or more, and partial seizures, with a variable degree of severity.

EXPRESSÃO TECIDUAL(Tecido-específico)
Brain Frontal Cortex BA9
15.1 TPM
Cérebro - Hemisfério cerebelar
10.7 TPM
Cerebelo
9.3 TPM
Córtex cerebral
8.9 TPM
Hipotálamo
6.3 TPM
OUTRAS DOENÇAS (13)
developmental and epileptic encephalopathy, 6Ageneralized epilepsy with febrile seizures plus, type 2developmental and epileptic encephalopathy 6Bfamilial hemiplegic migraine
HGNC:10585UniProt:P35498
ATP1A2Sodium/potassium-transporting ATPase subunit alpha-2Disease-causing germline mutation(s) inTolerante
FUNÇÃO

This is the catalytic component of the active enzyme, which catalyzes the hydrolysis of ATP coupled with the exchange of sodium and potassium ions across the plasma membrane. This action creates the electrochemical gradient of sodium and potassium, providing the energy for active transport of various nutrients

LOCALIZAÇÃO

MembraneCell membrane

VIAS BIOLÓGICAS (3)
Ion homeostasisIon transport by P-type ATPasesPotential therapeutics for SARS
MECANISMO DE DOENÇA

Migraine, familial hemiplegic, 2

A subtype of migraine with aura associated with hemiparesis in some families. Migraine is a disabling symptom complex of periodic headaches, usually temporal and unilateral. Headaches are often accompanied by irritability, nausea, vomiting and photophobia, preceded by constriction of the cranial arteries. Migraine with aura is characterized by recurrent attacks of reversible neurological symptoms (aura) that precede or accompany the headache. Aura may include a combination of sensory disturbances, such as blurred vision, hallucinations, vertigo, numbness and difficulty in concentrating and speaking.

OUTRAS DOENÇAS (7)
migraine, familial hemiplegic, 2fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic faciesdevelopmental and epileptic encephalopathy 98alternating hemiplegia of childhood 1
HGNC:800UniProt:P50993

Medicamentos e terapias

ACETAMINOPHENPhase 4

Mecanismo: Cyclooxygenase inhibitor

CAFFEINEPhase 4

Mecanismo: Adenosine receptor antagonist

ZOLMITRIPTANPhase 4

Mecanismo: Serotonin 1b (5-HT1b) receptor agonist

DIHYDROERGOTAMINE MESYLATEPhase 4

Mecanismo: Serotonin 1d (5-HT1d) receptor agonist

ALMOTRIPTAN MALATEPhase 4

Mecanismo: Serotonin 1b (5-HT1b) receptor agonist

NARATRIPTAN HYDROCHLORIDEPhase 4

Mecanismo: Serotonin 1d (5-HT1d) receptor agonist

DICLOFENAC POTASSIUMPhase 4

Mecanismo: Cyclooxygenase inhibitor

Ver mais no OpenTargets

Variantes genéticas (ClinVar)

5,004 variantes patogênicas registradas no ClinVar.

🧬 CACNA1A: NM_001127222.2(CACNA1A):c.2056G>C (p.Gly686Arg) ()
🧬 CACNA1A: NM_001127222.2(CACNA1A):c.5084G>A (p.Cys1695Tyr) ()
🧬 CACNA1A: NM_001127222.2(CACNA1A):c.1782-1G>A ()
🧬 CACNA1A: NM_001127222.2(CACNA1A):c.4979G>T (p.Arg1660Leu) ()
🧬 CACNA1A: NM_001127222.2(CACNA1A):c.5081T>A (p.Val1694Asp) ()
Ver todas no ClinVar

Diagnóstico

Os sinais que médicos procuram e os exames que confirmam

Carregando...

Tratamento e manejo

Remédios, cuidados de apoio e o que precisa acompanhar

Pipeline de tratamentos
Pipeline regulatório — de medicamentos já aprovados a drogas em pesquisa exploratória.
Aprovado7
Medicamentos catalogadosEnsaios clínicos· 7 medicamentos · 0 ensaios
✓ Aprovados — podem ser usados hoje
ACETAMINOPHENCAFFEINEZOLMITRIPTANDIHYDROERGOTAMINE MESYLATEALMOTRIPTAN MALATENARATRIPTAN HYDROCHLORIDEDICLOFENAC POTASSIUM
Carregando informações de tratamento...

Onde tratar no SUS

Hospitais de referência no Brasil e o protocolo oficial do SUS (PCDT)

🇧🇷 Atendimento SUS — Cefaleia hípica

🗺️

Selecione um estado ou use sua localização para ver resultados.

Dados de DATASUS/CNES, SBGM, ABNeuro e Ministério da Saúde. Sempre confirme a disponibilidade diretamente com o estabelecimento.

Pesquisa ativa

Ensaios clínicos abertos e novidades científicas recentes

Pesquisa e ensaios clínicos

Nenhum ensaio clínico registrado para esta condição.

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Publicações mais relevantes

Timeline de publicações
52 papers (10 anos)
#1

Rare Primary Headaches in Children: A Narrative Review.

Biomedicines2026 Jan 28

Headache is a very common disorder in children and adolescents. While migraine and tension headaches are well-known and diagnosed by pediatricians, a group of primary headaches in children, rare in frequency, are poorly understood and likely underestimated by physicians, resulting in delayed diagnosis and treatment. This review aims to provide an updated overview of these clinical forms, considering new evidence. We will present the main clinical, therapeutic, and pathophysiological aspects and possible future hypotheses, with specific reference to pediatric cases of the following clinical forms: cough headache, thunderclap headache, cold headache, primary stabbing headache, nummular headache, hypnic headache, red ear syndrome, and non-odontogenic orofacial pain. These clinical forms currently pose a major diagnostic challenge for pediatricians and represent a source of serious disability for children and adolescents.

#2

Pathofysiological and clinical correlates of sleep in primary headache disorders: A narrative review.

Sleep medicine2026 Feb 16

Sleep and headache are strongly interconnected, this narrative review gives an overview of the current pathophysiological and clinical correlates of sleep in primary headache disorders. Circuits across the brainstem and hypothalamus that are involved in the regulation of sleep and wake overlap with known headache and pain pathways, offering a possible pathophysiological basis for this relationship. Furthermore, growing evidence supports a key role for orexin (hypocretin), with dysregulated signalling and widespread orexin receptor expression in the trigeminocervical complex and trigeminal ganglion, key structures in headache pathophysiology. Clinically, people with migraine frequently report poor subjective sleep quality, high rates of insomnia, and an increased prevalence of sleep disorders such as restless legs syndrome. Additionally, reduced sleep is often reported as a trigger for migraine attacks. Cluster headache (CH) shows a particularly close relationship with sleep with attacks that occur at night during sleep. Polysomnography studies did not provide evidence for an association between specific sleep stages and attacks. Nonetheless, attacks often lead to impaired sleep quality and excessive daytime sleepiness in people with CH. Hypnic headache (HH) is characterized by headache attacks that occur exclusively during sleep. Lastly, sleep disturbances are also common in people with tension-type headache (TTH), particularly insomnia and daytime sleepiness. However, objective sleep studies generally show normal sleep architecture. Overall, substantial (patho)physiological and clinical overlap between headache and sleep disorders highlights the importance of systematically assessing and addressing of sleep disturbances in people with headache.

#3

Hallmarks of primary headache: part 4 - rare headache syndromes.

The journal of headache and pain2025 Dec 23

“Other primary headaches” is a group of heterogeneous headache disorders described in Chapter 4 of the third edition of the International Classification of Headache Disorders (ICHD-III). Due to the limited number of cases, most of these disorders are considered rare and represent a diagnostic and therapeutic challenge for clinicians and headache specialists. To increase knowledge, improve their recognition, and foster research on these rare headache disorders, this review provides a comprehensive up-to-date description of their hallmarks, including epidemiologic data, key clinical characteristics, proposed pathophysiological mechanisms, and suggested treatments. Diagnosing rare headache disorders is challenging. A few key clinical features can help improve their recognition and distinction. These include identifying a specific trigger or stimulus for headache development such as cough, exercise, or sexual activity, a particular pattern of onset or recurrence, like for hypnic headache, primary thunderclap headache, or new daily persistent headache, or a unique scalp location for the pain such as for nummular headache or epicrania fugax. These clinical details are crucial for narrowing the differential diagnosis and making the correct diagnosis. However, regardless of the specificity of the clinical presentation, secondary causes must be ruled out when facing patients with these rare clinical presentations. Limited evidence on the pathophysiology and treatment of these disorders is available, and high-quality studies are lacking. Accurate diagnosis and additional research on these rare headache disorders are needed. Multicenter and international collaborations within the framework of international headache societies and among tertiary headache centers are key to developing efficient and high-quality registries and databases. Additionally, clinical trials are needed to develop evidence supporting the treatments current in use and to address the unmet needs of these rare diseases. Only through these efforts it will be possible to design specific studies to increase our understanding of these rare disorders and improve the quality of life of individuals living with these conditions. Headache disorders are among the leading causes of morbidity and years lived with disability worldwide. Headaches have been classified into various categories based on the International Classification of Headache Disorders Criteria. Hypnic headache (HH) is a rare, primary headache disorder that occurs exclusively during sleep, usually simultaneously each night. Previously, HH was referred to as "the clockwise headache" or "alarm clock headache." The International Classification of Headache Disorders, 3rd ed classifies hypnic headache as a primary headache disorder. HH is characterized by attacks of dull headache that typically present after age 50, occur at least 10 times per month, and occur during sleep without associated autonomic symptoms. The attacks awaken the patient from sleep and usually last 15 minutes to 4 hours after waking. Hypnic headache is a chronic disorder that can last for many years, but has moderate remission rates with treatment. Patients with migraine and hypertension are more likely to develop HH. Nearly all patients with HH exhibit motor activity during the attack, such as getting out of bed, eating, drinking, showering, or reading when awakened by the headache. However, the restlessness is less severe than cluster headache and trigeminal autonomic cephalalgias. Other causes of nocturnal headache and secondary headaches should be excluded before confirming a diagnosis of HH.

#4

Nighttime Primary Headaches in Children: Beyond Hypnic Headache, a Comprehensive Review.

Life (Basel, Switzerland)2025 Jul 28

Many headaches at night arise due to primary headache disorders, which occur independently of other symptoms and are not caused by another medical condition. Primary headache disorders with nighttime attacks can include tension-type headaches, migraines, hypnic headaches, and cluster headaches. A hypnic headache is sometimes called an "alarm clock headache" because symptoms tend to arise at the same time of night. Apart from considering primary headaches, secondary causes of nighttime headaches should be considered and ruled out, in particular headaches secondary to intracranial hypertension, temporomandibular joint issues (like bruxism) and sleep apnea. Treatments vary based on headache type but often include a combination of medications and prevention strategies. This review article covers the basics of nighttime primary headaches in children, including pathophysiology, etiology, clinical features of the different forms and their treatment. It will also discuss the differences in headache features between children and adults.

#5

Co-morbid Indomethacin-Responsive Headaches in a Woman in Her Late 60s With Paroxysmal Hemicrania and Hypnic Headache: A Case Report.

Cureus2025 Jan

Paroxysmal hemicrania (PH) and hypnic headache (HH) are rare indomethacin-responsive headache syndromes. This case report details the new onset of both disorders in a woman in her late 60s. One headache type presented as severe pain centered on the right eyebrow, lasting 30 minutes, occurring more than 8 times daily, and associated with ipsilateral lacrimation and rhinorrhea. The second type was a right frontal severe pain, with onset at 4 a.m., occurring only during sleep, lasting 30 minutes, and with no associated factors. The patient's response to indomethacin for both headache types was confirmed through an unblinded ABAB study design: complete resolution of headaches during indomethacin use and recurrence upon discontinuation. This case highlights the rarity of co-morbid indomethacin-responsive headaches and underscores the diagnostic and therapeutic challenges associated with these conditions.

Publicações recentes

Ver todas no PubMed

📚 EuropePMC116 artigos no totalmostrando 49

2026

Rare Primary Headaches in Children: A Narrative Review.

Biomedicines
2026

Pathofysiological and clinical correlates of sleep in primary headache disorders: A narrative review.

Sleep medicine
2025

Hallmarks of primary headache: part 4 - rare headache syndromes.

The journal of headache and pain
2025

Nighttime Primary Headaches in Children: Beyond Hypnic Headache, a Comprehensive Review.

Life (Basel, Switzerland)
2025

Co-morbid Indomethacin-Responsive Headaches in a Woman in Her Late 60s With Paroxysmal Hemicrania and Hypnic Headache: A Case Report.

Cureus
2023

Headache providers' perspectives of headache diaries in the era of increasing technology use: a qualitative study.

Frontiers in neurology
2024

Images: Sleep-related painful erection with concomitant hypnic headache.

Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine
2023

Epidemiology and clinical features of hypnic headache: A systematic review and meta-analysis.

Cephalalgia : an international journal of headache
2023

Pediatric hypnic headache: a systematic review.

Frontiers in neurology
2023

Caffeine for Headaches: Helpful or Harmful? A Brief Review of the Literature.

Nutrients
2023

Case report: Hypnic headache responds to agomelatine-a potential prophylactic treatment option.

Frontiers in neurology
2023

Hypnic Headache - What do we know in 2022?

Cephalalgia : an international journal of headache
2023

Ecchordosis physaliphora presenting as hypnic headache.

The neuroradiology journal
2022

Greater occipital nerve (GON) blocks for treating of hypnic headache: A case report.

Sleep medicine
2022

Oxygen Therapy in Cluster Headache, Migraine, and Other Headache Disorders.

Journal of clinical neurology (Seoul, Korea)
2021

Hypnic Headache: A Rare Primary Headache Syndrome in an Indian Population with a Mini Review of Literature.

Neurology India
2021

Headache Associated with Sexual Activity-A Narrative Review of Literature.

Medicina (Kaunas, Lithuania)
2021

Beyond chronic migraine: a systematic review and expert opinion on the off-label use of botulinum neurotoxin type-A in other primary headache disorders.

Expert review of neurotherapeutics
2021

Uncommon (Group 4.0) Primary Headaches: Less Familiarity and More Missed Diagnosis.

Neurology India
2021

Hypnic Headache Responds to Topiramate: A Case Report and a Review of Mechanisms of Action of Therapeutic Agents.

Cureus
2021

The Potential Role of the Glymphatic System in Headache Disorders.

Pain medicine (Malden, Mass.)
2021

Acoustic neuroma presenting as a hypnic headache.

BMJ case reports
2020

The prevalence of hypnic headache in Iceland.

Cephalalgia : an international journal of headache
2019

Other Primary Headaches: An Update.

Neurologic clinics
2019

Hypnic Headache Due to Hypoglycemia: A Case Report.

Headache
2019

Hypnic headache: A review of 348 cases published from 1988 to 2018.

Journal of the neurological sciences
2019

Sleep disorder-related headaches.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
2019

Hypnic Headache with Dopaminergic Neuron Dysfunction: New Insight from a Rare Case.

Pain medicine (Malden, Mass.)
2018

Unusual Headache Disorders.

Continuum (Minneapolis, Minn.)
2019

Emerging relevance of circadian rhythms in headaches and neuropathic pain.

Acta physiologica (Oxford, England)
2018

Common Primary and Secondary Causes of Headache in the Elderly.

Headache
2017

Case report of hypnic headache: a rare headache disorder with nocturnal symptoms.

BMC research notes
2018

Sleep, chronic pain, and opioid risk for apnea.

Progress in neuro-psychopharmacology &amp; biological psychiatry
2017

No Pattern Alteration in Single Nocturnal Melatonin Secretion in Patients With Hypnic Headache: A Case-Control Study.

Headache
2016

The Role of Caffeine in Pain Management: A Brief Literature Review.

Anesthesiology and pain medicine
2017

Sleep disorders and chronic craniofacial pain: Characteristics and management possibilities.

Sleep medicine reviews
2016

The Role of Melatonin in the Treatment of Primary Headache Disorders.

Headache
2017

Case report of an alleviation of pain symptoms in hypnic headache via greater occipital nerve block.

Cephalalgia : an international journal of headache
2016

Case Report: Coexistence of SUNCT and Hypnic Headache in the Same Patient.

Headache
2016

Primary headache syndromes in the elderly: epidemiology, diagnosis and treatment.

Journal of clinical and translational research
2016

Long-Term Outcomes and Clinical Characteristics of Hypnic Headache Syndrome: 40 Patients Series From a Tertiary Referral Center.

Headache
2015

European Headache Federation consensus on technical investigation for primary headache disorders.

The journal of headache and pain
2015

Hypnic Headache and Basilar Artery Dolichoectasia.

The neurologist
2015

Unique Migraine Subtypes, Rare Headache Disorders, and Other Disturbances.

Continuum (Minneapolis, Minn.)
2015

Hypnic headache in childhood: A literature review.

Journal of the neurological sciences
2015

A Case of Unilateral Hypnic Headache: Rapid Response to Ramelteon, a Selective Melatonin MT1/MT2 Receptor Agonist.

Headache
2017

Influenza A virus: A possible trigger factor for hypnic headache?

Neurologia (Barcelona, Spain)
2015

Headaches of the elderly.

Current neurology and neuroscience reports
2016

[Hypnic headache, a case report].

Semergen
Ver todos os 116 no EuropePMC

Associações

Organizações que acompanham esta doença — pra ter apoio e orientação

Ainda não temos associações cadastradas para Cefaleia hípica.

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Comunidades

Grupos ativos de quem convive com esta doença aqui no Raras

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Doenças relacionadas

Doenças com sintomas parecidos — ajudam quem ainda está buscando diagnóstico

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.

  1. Rare Primary Headaches in Children: A Narrative Review.
    Biomedicines· 2026· PMID 41751188mais citado
  2. Pathofysiological and clinical correlates of sleep in primary headache disorders: A narrative review.
    Sleep medicine· 2026· PMID 41713202mais citado
  3. Hallmarks of primary headache: part 4 - rare headache syndromes.
    The journal of headache and pain· 2025· PMID 41430557mais citado
  4. Nighttime Primary Headaches in Children: Beyond Hypnic Headache, a Comprehensive Review.
    Life (Basel, Switzerland)· 2025· PMID 40868846mais citado
  5. Co-morbid Indomethacin-Responsive Headaches in a Woman in Her Late 60s With Paroxysmal Hemicrania and Hypnic Headache: A Case Report.
    Cureus· 2025· PMID 39925537mais citado
  6. Hypnic Headache.
    · 2026· PMID 32491530recente

Bases de dados e fontes oficiais

Identificadores e referências canônicas usadas para montar este verbete.

  1. ORPHA:276429(Orphanet)
  2. MONDO:0017181(MONDO)
  3. GARD:10796(GARD (NIH))
  4. Variantes catalogadas(ClinVar)
  5. Busca completa no PubMed(PubMed)
  6. Q54927701(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

Cefaleia hípica
Compêndio · Raras BR

Cefaleia hípica

ORPHA:276429 · MONDO:0017181
Prevalência
Unknown
Herança
Not applicable
CID-10
G44.8 · Outras síndromes de cefaléia especificadas
CID-11
Medicamentos
7 registrados
Início
Adult, Childhood, Elderly
Prevalência
0.0 (Worldwide)
MedGen
UMLS
C0752150
Repurposing
14 candidatos
acetylcholineacetylcholine receptor agonist
aspirincyclooxygenase inhibitor
butalbitalGABA receptor antagonist
+11 outros
EuropePMC
Wikidata
Papers 10a
DiscussaoAtiva

Nenhuma novidade ainda. O agente esta monitorando.

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