Neurol India Home 
 

BRIEF REPORT
Year : 2007  |  Volume : 55  |  Issue : 1  |  Page : 78--79

Huntington«SQ»s disease in all (three) siblings and their one parent

Roshan Lal Koul 
 Department of Child Health, Sultan Qaboos University Hospital, Muscat, Sultanate of Oman

Correspondence Address:
Roshan Lal Koul
Department of Child Health, Sultan Qaboos University Hospital, Muscat, Sultanate of Oman

Three siblings (two girls and one boy) and their father are reported who developed Huntington«SQ»s disease (HD). The two girls had onset at less than six years of age, while the boy started with symptoms at 12 years of age. The girl, the child number two, has expired and the youngest one is in a vegetative state. The elder brother is still mildly affected. The disease presented in a severe form and early in the females while it remained mild and presented late in the males. This is a rare disease involving all the three surviving siblings and their father. The diagnosis was confirmed after genetic testing.


How to cite this article:
Koul RL. Huntington's disease in all (three) siblings and their one parent.Neurol India 2007;55:78-79


How to cite this URL:
Koul RL. Huntington's disease in all (three) siblings and their one parent. Neurol India [serial online] 2007 [cited 2021 Oct 24 ];55:78-79
Available from: https://www.neurologyindia.com/article.asp?issn=0028-3886;year=2007;volume=55;issue=1;spage=78;epage=79;aulast=Koul;type=0