Usher syndrome: A case report;Le syndrome de usher: À propos d'une observation

Revue Neurologique

Volumn 159, Issue 3, 2003, Pages 323-325

  Drouet, A ^a   Swalduz, B ^b   Guilloton, L ^a   Faivre, A ^a   Felten, D ^a  

^a Service de Neurologie   (France)

^b Service d'Ophtalmologie   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; ATAXIA; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; CEREBELLUM ATROPHY; DISEASE EXACERBATION; DISEASE SEVERITY; FEMALE; HUMAN; JEW; PERCEPTION DEAFNESS; RETINOPATHY; USHER SYNDROME; VESTIBULAR FUNCTION; VISUAL IMPAIRMENT;

BRAIN; CONSANGUINITY; DIAGNOSIS, DIFFERENTIAL; ELECTRORETINOGRAPHY; FEMALE; FUNDUS OCULI; HEARING LOSS, SENSORINEURAL; HUMANS; MAGNETIC RESONANCE IMAGING; MEMBRANE PROTEINS; MIDDLE AGED; RETINITIS PIGMENTOSA; SYNDROME;

EID: 0344211934     PISSN: 00353787     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

1. KEATS BJB, COREY DP. (1999). The Usher syndromes. Am J Med Genet, 89: 158-166.
2. LYNCH SG, DIGRE K, ROSE JW. (1994). Usher's syndrome and multiple sclerosis. Review of an individual with Usher's syndrome with a multiple sclerosis-like illness. J Neuro Ophtalmol, 14: 34-37.
3. PIAZZA L, FISHMAN GA, KAPLAN RD, HOROWITZ A, HINDO WA, MAFEE MF. (1987). Magnetic resonance imaging of central nervous system defects in Usher's syndrome. Retina, 7: 271-245.
4. TAMAYO ML, MALDONADO C, PLAZA SL et al. (1996). Neuroradiology and clinical aspects of Usher syndrome. Clin Genet, 50: 126-132.
5. USHER CH. (1914). On the inheritance of retinitis pigmentosa with notes of the cases. R Lond Ophtalmol Hop Resp, 10: 130-256.
6. VON GRAEFE A. (1858). Exceptionelles Verhalten des Gesichtsfeldes bei pigmententarung der Netzhaut. Von Graefe's Arch Klin Exp Ophtalmol, 4: 250-253.