BRACHMANN-DELANGE SYNDROME - DIAGNOSTIC DIFFICULTIES POSED BY THE MILD PHENOTYPE

被引:16
作者
SAUL, RA
ROGERS, RC
PHELAN, MC
STEVENSON, RE
机构
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1993年 / 47卷 / 07期
关键词
BRACHMANN-DELANGE SYNDROME; PHENOTYPIC VARIATION;
D O I
10.1002/ajmg.1320470712
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We describe 4 patients with facial changes of Brachmann-de Lange syndrome but without limb defects. Mental retardation ranged from moderate to severe and the degree of prenatal and postnatal growth deficiency was variable. These patients exemplify the diagnostic difficulties and counseling dilemmas posed by the mild Brachmann-de Lange phenotype. The relationship of the mild phenotype to the full syndrome will not be understood until the pathogenetic or causal factor(s) are delineated. (C) 1993 Wiley-Liss, Inc.
引用
收藏
页码:999 / 1002
页数:4
相关论文
共 22 条
[1]   FAMILIAL OCCURRENCE OF BRACHMANN DE-LANGE-SYNDROME [J].
BANKIER, A ;
HAAN, E .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 25 (01) :163-165
[2]   FAMILIAL OCCURRENCE OF CORNELIA-DELANGES SYNDROME [J].
BECK, B .
ACTA PAEDIATRICA SCANDINAVICA, 1974, 63 (02) :225-231
[3]  
Brachmann W., 1916, JB KINDERHEILK PHYS, V84, P225
[4]  
BRESLAU EJ, 1981, AM J MED GENET, V1, P179
[5]  
De Lange C., 1933, ARCHIVES MEDICIN ENF, V36, P713
[6]  
FILIPPI G, 1989, CLIN GENET, V35, P343
[7]   CHROMOSOME 3Q DUPLICATION AND THE BRACHMANN-DELANGE SYNDROME (BDLS) [J].
FRANCKE, U ;
OPITZ, JM .
JOURNAL OF PEDIATRICS, 1979, 95 (01) :161-162
[8]  
FRYNS JP, 1987, CLIN GENET, V31, P413
[9]   MILD BRACHMANN-DELANGE SYNDROME - CHANGES OF PHENOTYPE WITH AGE [J].
GREENBERG, F ;
ROBINSON, LK .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 32 (01) :90-92
[10]   64 PATIENTS WITH BRACHMANN-DE-LANGE SYNDROME - A SURVEY [J].
HAWLEY, PP ;
JACKSON, LG ;
KURNIT, DM .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 20 (03) :453-459