Kjellin syndrome;Syndrome de kjellin

Revue Neurologique

Volumn 157, Issue 1, 2001, Pages 80-83

  Ferriby, D ^a   Stojkovic, T ^a   De Seze, J ^a   Puech, B ^a   Josien, E ^b   Hache, J C ^a   Vermersch, P ^a  

^a LILLE UNIVERSITY HOSPITAL   (France)

^b Service de Neurologie   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; BRAIN DISEASE; CASE REPORT; CLINICAL FEATURE; COGNITIVE DEFECT; DIFFERENTIAL DIAGNOSIS; DISEASE ASSOCIATION; DISEASE COURSE; FEMALE; HUMAN; KJELLIN SYNDROME; RETINA MACULA LUTEA; SPASTIC PARESIS; SYNDROME; VISUAL IMPAIRMENT;

ADULT; FEMALE; HUMANS; MACULAR DEGENERATION; MENTAL RETARDATION; PARAPARESIS, SPASTIC; SYNDROME; VISION DISORDERS;

EID: 0035137230     PISSN: 00353787     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (9)

1. Flecked retina disorders
2. Fleck retina in Kjellin's syndrome
3. Fleck retina
4. Familial spastic paraplegia with amyotrophy, oligophrenia, and central retinal degeneration
5. Flecked retina syndrome
6. The hereditary spastic paraplegias
7. Zur pathologie und pathologischen histology der spastichen heredodegeneration (hereditäre spastische spinalparalyse)
8. Hereditary spastic paraplegia with retinal disease