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This study investigated what proportion of autosomal recessive condition characterized by deafness and goitre were due to mutation of the Pendred syndrome gene
Abstract:
Although the textbook view of Pendred syndrome is that of an autosomal recessive condition characterized by deafness and goitre, it is increasingly clear that not all such patients present this classical clinical picture. Malformations of the inner ear, specifically enlargement of the vestibular aqueduct, are common in Pendred syndrome and mutations in the PDS (Pendred Syndrome) gene more...
International Classification:
Syndrome - Pendred
Categories:
Pendred syndrome
Geography:
Republic of Ireland and the United Kingdom
Qjm,
Vol: 93 Page: 99-104 February 2000
W. Reardon; O. Mahoney CF ; R. Trembath; H. Jan; P. D. Phelps
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