Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome)

Orphanet Journal of Rare Diseases

Volumn 3, Issue 1, 2008, Pages

  Desir, Julie ^a   Abramowicz, Marc ^a  

^a ERASME HOSPITAL   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AUDIOMETRY; CHILD; CONGENITAL CORNEA DYSTROPHY; CORNEA TRANSPLANTATION; FEMALE; GENETICS; HUMAN; MALE; PATHOPHYSIOLOGY; PERCEPTION DEAFNESS; PRESCHOOL CHILD; REVIEW;

ADOLESCENT; ADULT; AUDIOMETRY; CHILD; CHILD, PRESCHOOL; CORNEAL DYSTROPHIES, HEREDITARY; CORNEAL TRANSPLANTATION; FEMALE; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; YOUNG ADULT;

EID: 55149103495     PISSN: None     EISSN: 17501172     Source Type: Journal    
DOI: 10.1186/1750-1172-3-28     Document Type: Review

References (43)

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