Kjellin syndrome: First case with retinal changes in carriers

Neurology

Volumn 65, Issue 7, 2005, Pages 1110-

  Sachdev, Arun ^a   Proudlock, Frank A ^a   Abbott, Richard ^a   Gottlob, Irene ^a,b  

^a Leicester Royal Infirmary ^*

^b UNIVERSITY OF LEICESTER   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; DEMENTIA; DYSARTHRIA; FEMALE; FLUORESCENCE ANGIOGRAPHY; HETEROZYGOTE; HUMAN; KJELLIN SYNDROME; OPHTHALMOSCOPY; PRIORITY JOURNAL; RETINA DISEASE; SPASTIC PARAPLEGIA;

EID: 26444542853     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.wnl.0000182290.78138.69     Document Type: Article

References (2)

1. Kjelllin K. Family spastic paraplegia with amyotrophy, oligophrenia, and central retinal degeneration. Arch Neurol 1959;1:133.
2. Farmer SG, Longstreth WT, Kalina RE, Todorov AB. Fleck retina in Kjellin's syndrome. Am J Ophthalmol 1985;99:45-50.