The Kennedy family and the story of mental retardation

2001 ◽  
Vol 37 (4) ◽  
pp. 422-423
Author(s):  
Leland V. Bell
Isis ◽  
2001 ◽  
Vol 92 (4) ◽  
pp. 814-815
Author(s):  
Steven Noll

JAMA ◽  
2001 ◽  
Vol 285 (14) ◽  
pp. 1893-1894
Author(s):  
P. E. Veenhuis

Author(s):  
Line Buhl ◽  
David Muirhead

There are four lysosomal diseases of which the neuronal ceroid lipofuscinosis is the rarest. The clinical presentation and their characteric abnormal ultrastructure subdivide them into four types. These are known as the Infantile form (Santavuori-Haltia), Late infantile form (Jansky-Bielschowsky), Juvenile form (Batten-Spielmeyer-Voght) and the Adult form (Kuph's).An 8 year old Omani girl presented wth myclonic jerks since the age of 4 years, with progressive encephalopathy, mental retardation, ataxia and loss of vision. An ophthalmoscopy was performed followed by rectal suction biopsies (fig. 1). A previous sibling had died of an undiagnosed neurological disorder with a similar clinical picture.


Sign in / Sign up

Export Citation Format

Share Document