A stepwise approach to the diagnosis and treatment of hereditary hearing loss

Pediatric Clinics of North America

Volumn 46, Issue 1, 1999, Pages 35-48

  Tomaski, S M ^a   Grundfast, K M ^a  

^a GEORGETOWN UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ALPORT SYNDROME; AUDIOGRAPHY; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL RECESSIVE DISORDER; CHILD; COMPUTER ASSISTED TOMOGRAPHY; DISEASE CLASSIFICATION; DISORDERS OF MITOCHONDRIAL FUNCTIONS; EDUCATION; FAMILY HISTORY; GENETIC DISORDER; HEARING AID; HEARING LOSS; HEARING TEST; HUMAN; INFANT; LONG QT SYNDROME; MANDIBULOFACIAL DYSOSTOSIS; NEUROFIBROMATOSIS; NEWBORN; NUCLEAR MAGNETIC RESONANCE IMAGING; PATIENT REFERRAL; PENDRED SYNDROME; PHYSICAL EXAMINATION; REVIEW; STICKLER SYNDROME; USHER SYNDROME; VESTIBULAR TEST; X CHROMOSOME LINKED DISORDER;

EID: 0032914401     PISSN: 00313955     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0031-3955(05)70079-1     Document Type: Article

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