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Branchio‐oto‐renal dysplasia associated with tetralogy of fallot
Author(s) -
Daggilas Angelos,
Antoniades Kostas,
Palasis Sousan,
Aidonis Athanasios
Publication year - 1992
Publication title -
head and neck
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.012
H-Index - 127
eISSN - 1097-0347
pISSN - 1043-3074
DOI - 10.1002/hed.2880140211
Subject(s) - medicine , tetralogy of fallot , dysplasia , sensorineural hearing loss , renal dysplasia , hearing loss , girl , pathology , dermatology , anatomy , heart disease , audiology , urinary system , biology , genetics
Branchio‐oto‐renal dysplasia in its full expression consists of external ear malformations, cervical fistulas or cysts, preauricular pits, hearing loss of conductive sensorineural or mixed type, and renal anomalies. The syndrome is inherited in an autosomal dominant mode. We present a sporadic case of BOR dysplasia associated with tetralogy of Fallot in a 30‐month‐old girl. The clinical aspects of the disease are discussed briefly.