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Neamhord meathlú inchinne a fhaightear le hoidhreacht. Tagann sí chun tosaigh go luath i mbeatha fhásta an duine mar néaltrú a fhásann go mall, agus gluaiseachtaí neamhshrianta preabacha nó lúbarnaíl mhall. Níl aon leigheas air. Ainmníodh í as an lia Meiriceánach George Sumner Huntington (1850-1916).[1]
Cineál | néaraimheathlúchán, galar Huntington agus galair ghaolmhara, galar meathlúcháin na súl, genetic neurodegenerative disease with dementia (en) , trinucleotide repeat disorder (en) agus galar |
---|---|
Eapainm | George Huntington |
Speisialtacht leighis | néareolaíocht |
Cóireáil chliniciúil | |
Comharthaí | athrú pearsantachta, falrais, cailleadh meáchain agus néaltrú |
Scrúduithe | genetic testing (en) |
Cógais pimozide (en) , (RS)-baclofen (en) , perphenazine (en) , ubidecarenone (en) , tetrabenazine (en) agus tetrabenazine (en) | |
Pataigineas | |
Cúis ghéiniteach | HTT |
Cúis | trinucleotide repeat expansion (en) |
Aicmiú | |
ICD-10 | G10 agus F02.2 |
ICD-9 | 333.4333.4,294.1294.1 |
CIAP | P70 |
Acmhainní seachtracha | |
OMIM | 143100 |
DiseasesDB | 6060 |
MedlinePlus | 000770 |
eMedicine | 1150165, 289706 agus 792600 |
Patient UK | huntingtons-disease |
MeSH | D006816 |
GeneReviews | Panoramica agus Panoramica |
Orphanet | 399 |
UMLS CUI | C0020179 |
DOID | DOID:12858 |
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