[Kjellin syndrome]. / Syndrome de Kjellin.
Rev Neurol (Paris)
; 157(1): 80-3, 2001 Jan.
Article
em Fr
| MEDLINE
| ID: mdl-11240552
ABSTRACT
A previously healthy 30-year-old woman who had cognitive impairment since childhood suddenly developed progressive spastic paraparesis. Visual impairment and characteristic retinal macular spots supported the diagnosis of Kjellin syndrome. This disease, probably transmitted by autosomal recessive inheritance, is seldom observed in clinical practice. We describe the characteristics of Kjellin syndrome and the differential diagnosis, including other macular changes associated with spastic paraparesis.
Buscar no Google
Base de dados:
MEDLINE
Assunto principal:
Transtornos da Visão
/
Paraparesia Espástica
/
Degeneração Macular
/
Deficiência Intelectual
Limite:
Adult
/
Female
/
Humans
Idioma:
Fr
Ano de publicação:
2001
Tipo de documento:
Article