About: Familial hemiplegic migraine

Facets (new session)
Description
Metadata
Settings
- Rule:
- Inverse Functional Properties:
- "Same As":

About: Familial hemiplegic migraine Goto Sponge NotDistinct Permalink

An Entity of Type : umbel-rc:AilmentCondition, within Data Space : dbpedia.demo.openlinksw.com associated with source document(s)
QRcode icon

http://dbpedia.demo.openlinksw.com/c/5pRiFkF4VA

Familial hemiplegic migraine (FHM) is an autosomal dominant type of hemiplegic migraine that typically includes weakness of half the body which can last for hours, days, or weeks. It can be accompanied by other symptoms, such as ataxia, coma, and paralysis. Migraine attacks may be provoked by minor head trauma. Some cases of minor head trauma in patients with hemiplegic migraine can develop into delayed cerebral edema, a life-threatening medical emergency. Clinical overlap occurs in some FHM patients with episodic ataxia type 2 and spinocerebellar ataxia type 6, benign familial infantile epilepsy, and alternating hemiplegia of childhood.

Attributes	Values
rdf:type	Thing Disease yago:Abstraction100002137 yago:Attribute100024264 yago:Cognition100023271 yago:Concern105832264 yago:Condition113920835 yago:Disease114070360 yago:IllHealth114052046 yago:Illness114061805 yago:Information105816287 yago:NegativeStimulus105829480 yago:PathologicalState114051917 yago:PhysicalCondition114034177 yago:PsychologicalFeature100023100 yago:WikicatHeadaches disease yago:State100024720 yago:Stimulation105827684 umbel-rc:AilmentCondition
rdfs:label	صداع نصفي فالجي عائلي (ar) Familial hemiplegic migraine (en) Migraine hémiplégique familiale (fr) Emicrania emiplegica familiare (it) Гемиплегическая мигрень (ru)
rdfs:comment	الصداع النصفي الفالجي العائلي أو الشقيقة الفالجية (بالإنجليزية: Familial hemiplegic migraine)‏ هو أحد أنواع الصداع النصفي الذي سببه صفة وراثية سائدة ويصاحبه خزل شقي من الممكن أن يستمر ساعات أو أياما أو أسابيع. ومن الأعراض التي من المحتمل ظهورها: رنح أو غيبوبة أو شلل. (ar) Familial hemiplegic migraine (FHM) is an autosomal dominant type of hemiplegic migraine that typically includes weakness of half the body which can last for hours, days, or weeks. It can be accompanied by other symptoms, such as ataxia, coma, and paralysis. Migraine attacks may be provoked by minor head trauma. Some cases of minor head trauma in patients with hemiplegic migraine can develop into delayed cerebral edema, a life-threatening medical emergency. Clinical overlap occurs in some FHM patients with episodic ataxia type 2 and spinocerebellar ataxia type 6, benign familial infantile epilepsy, and alternating hemiplegia of childhood. (en) La migraine hémiplégique familiale est une forme rare de migraine avec aura. Dans ce type de migraine, les manifestations neurologiques sont celles d'une atteinte du cortex ou du tronc cérébral et comprennent des troubles de la vision, des déficits sensoriels (paresthésie de la face ou des extrémités) et des troubles de la parole. Mais la migraine hémiplégique familiale se caractérise, en plus de ces symptômes, par des signes d'atteintes motrices comme une hémiparésie. On distingue au moins trois types de migraine hémiplégique familiale : (fr) L'emicrania emiplegica familiare è una rara malattia genetica autosomica dominante, caratterizzata da attacchi di emicrania che comprendono tipicamente emiparesi (debolezza della metà del corpo) che può durare per ore, giorni o settimane. Essa può essere considerata come una variante più grave dell'emicrania con aura, accompagnata da altri sintomi, come l'atassia, il coma e la paralisi. Ci sono 3 loci noti per la condizione: FHM1, che rappresenta circa il 50% dei pazienti ed è causata da mutazioni in un gene che codifica per un canale del calcio P/Q α subunità, CACNA1A. FHM1 è anche associato a degenerazione cerebellare. FHM2, che rappresenta meno dei 25% dei casi di emicrania emiplegica familiare, ed è causata da mutazioni gene ATPasi della pompa sodio-potassio. L'FHM3 è un raro sottotipo (it) Гемиплегическая мигрень — относительно редкая разновидность мигрени, при которой появляется повторяющаяся временная слабость с одной стороны тела (гемиплегия — понятие, обозначающее паралич мышц одной половины тела). (ru)
foaf:name	Familial hemiplegic migraine (en)
name	Familial hemiplegic migraine (en)
foaf:depiction
dct:subject	Rare diseases Channelopathies Headaches
Wikipage page ID	4206029 (xsd:integer)
Wikipage revision ID	1081648703 (xsd:integer)
Link from a Wikipage to another Wikipage	Benign familial infantile epilepsy Electrophysiology Mitochondrial disease Mutation Nucleotide Oocyte CACNA1A Hypokalemic periodic paralysis Pathologic nystagmus De novo mutation Neurotransmitter Penetrance Coma Concussion SPECT Gene knockout Nausea Neuron PRRT2 Episodic ataxia Na+/K+-ATPase Convulsion MRI Malignant hyperthermia Calcium channel Stroke Hemiparesis Autosomal dominant Action potential Cerebellum G protein-coupled receptor Ion channel Ion transporter Juvenile myoclonic epilepsy Locus (genetics) dbr:Acetazolamide dbr:Adenosine Amino acid Alternating hemiplegia of childhood Exocytosis Chromosome 1 Haploinsufficiency Isoform Rare diseases ATP1A2 Hemiplegic migraine Astrocyte Ataxia Timothy syndrome Channelopathies Headaches Childhood absence epilepsy Aura (symptom) Axon CADASIL Spinocerebellar ataxia Sporadic hemiplegic migraine FHM2 Migraine National Center for Biotechnology Information Rabbit Cerebral edema

Faceted Search & Find service v1.17_git147 as of Sep 06 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 08.03.3331 as of Sep 2 2024, on Linux (x86_64-generic-linux-glibc212), Single-Server Edition (378 GB total memory, 59 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software