Andermann syndrome in an Algerian family: Suggestion of phenotypic and genetic homogeneity;Le syndrome d'Andermann dans une famille algérienne: Suggestion d'une homogénéité phénotypique et génétique

Revue Neurologique

Volumn 157, Issue 10, 2001, Pages 1279-1281

  Lesca, G ^a   Cournu Rebeix, I ^a   Azoulay Cayla, A ^a   Lyon Caen, O ^a   Barois, A ^b   Dulac, O ^c   Fontaine, B ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b RAYMOND POINCARÉ HOSPITAL   (France)

^c HÔPITAL SAINT VINCENT DE PAUL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ALGERIA; ANDERMANN SYNDROME; ARTICLE; CANADA; CASE REPORT; CHROMOSOME 15Q; CORPUS CALLOSUM AGENESIS; GENE LOCUS; GENOTYPE; HAPLOTYPE; HOMOZYGOSITY; HUMAN; MARKER GENE; POLYNEUROPATHY; SIBLING;

EID: 0035160395     PISSN: 00353787     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (7)

1. Familial agenesis of the corpus callosum with anterior horn cell disease. A syndrome of mental retardation, areflexia, and paraplegia
2. The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q
3. Genetic epidemiology of sensorimotor polyneuropathy with or without agenesis of the corpus callosum in north-eastern Québec
4. Familial progressive sensorymotor neuropathy with agenesis of the corpus callosum (Andermann syndrome): A clinical, radiological and histopathological study
5. Occurrence of Andermann syndrome out of French Canada: Agenesis of the corpus callosum with neuronopathy
6. The Andermann syndrome: Agenesis of the corpus callosum associated with mental retardation and progressive sensorimotor neuronopathy
7. Neuropathie sensitivomotrice héréditaire avec ou sans agénésie du corps calleux: Étude radiologique et clinique de 64 cas