Ocular findings in Alport syndrome: 32 Case studies;Atteinte oculaire au cours du syndrome d'Alport. À propos de 32 cas

Journal Francais d'Ophtalmologie

Volumn 31, Issue 6, 2008, Pages 597-604

  Hentati, N ^a,d   Sellami, D ^a   Makni, K ^b   Kharrat, M ^c   Hachicha, J ^c   Hammadi, A ^b   Feki, J ^a  

^a HABIB BOURGUIBA HOSPITAL   (Tunisia)

^b CENTRE DE BIOTECHNOLOGIE DE SFAX   (Tunisia)

^c HEDI CHAKER HOSPITAL   (Tunisia)

^d NONE   (Tunisia)

Author keywords

Alport syndrome; Anterior lenticonus; Hereditary; Hereditary nephritis

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; CATARACT; CONGENITAL MALFORMATION; CORNEA DISEASE; DOMINANT GENE; EYE DISEASE; FEMALE; GENETICS; HUMAN; LENS; LENS DISEASE; MALE; MIDDLE AGED; NEPHRITIS; PATHOLOGY; RECESSIVE GENE; RETINA DISEASE; RETINITIS PIGMENTOSA; TUNISIA; VISUAL ACUITY; VISUAL DISORDER; X CHROMOSOMAL INHERITANCE;

ADOLESCENT; ADULT; AGED; CATARACT; CORNEAL DISEASES; EYE DISEASES; FEMALE; GENES, DOMINANT; GENES, RECESSIVE; GENES, X-LINKED; HUMANS; LENS DISEASES; LENS, CRYSTALLINE; MALE; MIDDLE AGED; NEPHRITIS, HEREDITARY; RETINAL DISEASES; RETINITIS PIGMENTOSA; TUNISIA; VISION DISORDERS; VISUAL ACUITY; YOUNG ADULT;

EID: 51049110932     PISSN: 01815512     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0181-5512(08)75461-5     Document Type: Article

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