COFFIN-LOWRY SYNDROME - CLINICAL ASPECTS AT DIFFERENT AGES AND SYMPTOMS IN FEMALE CARRIERS

被引:0
|
作者
PLOMP, AS
DEDIESMULDERS, CEM
MEINECKE, P
YPMAVERHULST, JM
LISSONE, DA
FRYNS, JP
机构
[1] ACAD HOSP MAASTRICHT,DEPT CLIN GENET,MAASTRICHT,NETHERLANDS
[2] ALTONA CHILDRENS HOSP,DEPT MED GENET,HAMBURG,GERMANY
[3] ST LAURENTIUS HOSP,DEPT PEDIAT,ROERMOND,NETHERLANDS
[4] UNIV HOSP LEUVEN,CTR HUMAN GENET,LOUVAIN,BELGIUM
[5] STICHTING WELZIJNSZORG GEESTELIJK GEHANDICAPTEN O,HEERLEN,NETHERLANDS
来源
GENETIC COUNSELING | 1995年 / 6卷 / 03期
关键词
COFFIN-LOWRY SYNDROME; MR SYNDROME; X-LINKED MENTAL RETARDATION; FEMALE HETEROZYGOTES;
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Coffin-Lowry syndrome: clinical aspects at different ages and symptoms in female carriers: We present three patients with the Coffin-Lowry syndrome, two males aged 21 years and 14 months respectively, and an unrelated girl aged 11 years. In the male patients the features at different ages are reviewed. Besides; we describe the pertinent features of their affected female relatives. The contribution of the family history to making the diagnosis is stressed. The isolated female proband is much more severely affected than the female relatives of the male probands, demonstrating that the clinical picture in female carriers of Coffin-Lowry syndrome can vary considerably. The differential diagnosis of Coffin-Lowry syndrome will be discussed shortly.
引用
收藏
页码:259 / 268
页数:10
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