Non-syndromal round window atresia: An autosomal dominant genetic disorder with variable penetrance?

European Archives of Oto-Rhino-Laryngology

Volumn 264, Issue 9, 2007, Pages 1103-1108

  Borrmann, A ^a   Arnold, W ^a  

^a TECHNICAL UNIVERSITY OF MUNICH   (Germany)

Author keywords

Genetic disorder; Round window atresia; Sound transmission

Indexed keywords

PENTOXIFYLLINE;

ADULT; ARTICLE; ATRESIA; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; COCHLEA FENESTRA; COMPUTER ASSISTED TOMOGRAPHY; DIZZINESS; EAR DISEASE; FAMILY; FEMALE; HEARING AID; HEARING LOSS; HEARING TEST; HUMAN; INNER EAR DISEASE; MIDDLE EAR; NONSYNDROMAL ROUND WINDOW ATRESIA; OTOSCLEROSIS; PERCEPTION DEAFNESS; POSTOPERATIVE PERIOD; PRIORITY JOURNAL; REOPERATION; STAPEDECTOMY; TINNITUS; TYMPANOMETRY; VESTIBULAR SYSTEM;

ADULT; EAR, MIDDLE; FAMILY HEALTH; FEMALE; GENES, DOMINANT; GENETIC PREDISPOSITION TO DISEASE; HEARING LOSS, BILATERAL; HEARING LOSS, CONDUCTIVE; HEARING TESTS; HUMANS; MALE; MODELS, GENETIC; PEDIGREE; PENETRANCE; ROUND WINDOW, EAR;

EID: 34547101195     PISSN: 09374477     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00405-007-0305-1     Document Type: Article

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