PLEIOTROPY IN COFFIN-LOWRY SYNDROME - SENSORINEURAL HEARING DEFICIT AND PREMATURE TOOTH LOSS AS EARLY MANIFESTATIONS

被引:27
作者
HARTSFIELD, JK
HALL, BD
GRIX, AW
KOUSSEFF, BG
SALAZAR, JF
HAUFE, SMW
机构
[1] UNIV KENTUCKY,COLL MED,DEPT PEDIAT,DIV GENET & DYSMORPHOL,LEXINGTON,KY 40506
[2] UNIV CALIF DAVIS,SACRAMENTO MED CTR,SCH MED,DEPT PEDIAT,SACRAMENTO,CA 95817
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1993年 / 45卷 / 05期
关键词
DEVELOPMENTAL DELAY; FACIAL CHANGES; PREMATURE EXFOLIATION;
D O I
10.1002/ajmg.1320450505
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report on 7 patients (6 M, 1 F) with Coffin-Lowry syndrome who have a sensorineural hearing deficit in addition to developmental delay and characteristic facial changes. One of the patients also had a history of premature exfoliation of primary teeth. These are previously unappreciated clinical signs that may aid in the early diagnosis of Coffin-Lowry syndrome. Early diagnosis and recognition of a hearing deficit in the patient can lead to the use of hearing aids to help the patient achieve his or her full potential. These ''new'' clinical manifestations expand the phenotype of Coffin-Lowry syndrome and constitute an additional indication of pleiotropy.
引用
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页码:552 / 557
页数:6
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