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PMID: 8533848 Published · ppublish English Journal Article Multicenter Study

Phenotypic manifestations of branchio-oto-renal syndrome.

American journal of medical genetics ·Vol. 58 ·No. 4 ·1995-09-25 ·Pages 365-70

Chen A, Francis M, Ni L, Cremers CW, Kimberling WJ, Sato Y, Phelps PD, Bellman SC, Wagner MJ, Pembrey M

Abstract

Branchiootorenal (BOR) syndrome is a variable, autosomal-dominant disorder of the first and second embryonic branchial arches, kidneys, and urinary tract. We describe the phenotype in 45 individuals, highlighting differences and similarities reported in other studies. Characteristic temporal bone findings include cochlear hypoplasia (4/5 of normal size with only 2 turns), dilation of the vestibular aqueduct, bulbous internal auditory canals, deep posterior fossae, and acutely-angled promontories.

MeSH Terms
Abnormalities, Multiple/genetics Branchial Region/abnormalities Ear/abnormalities Female Hearing Loss/genetics Humans Kidney/abnormalities Male Pedigree Phenotype Syndrome Urinary Tract/abnormalities
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Chen A
Department of Otolaryngology-Head and Neck Surgery, University of Iowa, Iowa City 52242, USA.
Francis M
Ni L
Cremers C W
Kimberling W J
Sato Y
Phelps P D
Bellman S C
Wagner M J
Pembrey M
Article Info
Journal
American journal of medical genetics
Abbr.
Am J Med Genet
ISSN
0148-7299
Published
1995-09-25
Pages
365-70
Language
English
Region
United States
NLM ID
7708900
Subset
IM
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