VARIABILITY OF THE BRACHMANN-DELANGE SYNDROME

被引:18
作者
SELICORNI, A
LALATTA, F
LIVINI, E
BRISCIOLI, V
PIGUZZI, T
BAGOZZI, DC
MASTROIACOVO, P
ZAMPINO, G
GAETA, G
PUGLIESE, A
CERUTTIMAINAROLI, P
GUALA, A
ZELANTE, L
STABILE, M
BELLI, S
FRANCESCHINI, P
GIANOTTI, A
SCARANO, G
机构
[1] UNIV MILAN,IST CLIN PERFEZIONAMENTO,PEDIAT CLIN 2,I-20122 MILAN,ITALY
[2] UCSC,SERV DIFETTI CONGENITI CLIN PEDIAT,ROME,ITALY
[3] IST INFANZIA BURLO GAROFOLO,TRIESTE,ITALY
[4] REPARTO TERAPIA INTENS NEONATALE OSPED CARDARELLI,NAPLES,ITALY
[5] USSL 45,DIV PEDIAT,VERCELLI,ITALY
[6] OSPED CSSS S GIOVANNI ROTONDO,SERV GENET MED,FOGGIA,ITALY
[7] OSPED CARDARELLI,SERV GRAVIDANZE RISCHIO,NAPLES,ITALY
[8] OSPED INFANTILE,TRENT,ITALY
[9] IST DISCIPLINE PEDIAT,SERV GENET CLIN,TURIN,ITALY
[10] OSPED BAMBINO GESU,SERV GENET MED,ROME,ITALY
[11] OSPED G MOSCATI,CTR GENET MED,AVELLINO,ITALY
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1993年 / 47卷 / 07期
关键词
BRACHMANN-DELANGE SYNDROME; DELANGE; CORNELIA; MILD PHENOTYPE; MENTAL RETARDATION; CLINICAL VARIABILITY; PHENOTYPIC HETEROGENEITY;
D O I
10.1002/ajmg.1320470708
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Brachmann-de Lange syndrome (BDLS) is a relatively common multiple congenital anomaly/mental retardation syndrome, whose cause is unknown. The clinical variability of this condition is well-known. Recently some reports suggested the possible existence of a mild BDLS phenotype. We report on 30 patients in whom a diagnosis of BDLS was made or strongly suspected in 12 different Italian hospitals. Based on clinical evaluation we divided them into two groups, classical and mild BDLS cases. We compare the clinical data of these patients and we discuss the problems which arise in trying to define clear criteria of distinction between these two groups. (C) 1993 Wiley-Liss, Inc.
引用
收藏
页码:977 / 982
页数:6
相关论文
共 48 条
[1]  
ALLERDICE PW, 1975, AM J HUM GENET, V27, P699
[2]  
BANKIER A, 1985, AM J MED GENET, V25, P163
[3]   NEUROLOGIC AND PSYCHOMETRIC FINDINGS IN BRACHMANN-DE LANGE SYNDROME [J].
BARR, AN ;
MATTHEWS, CG ;
GRABOW, JD ;
GROSSE, FR ;
OPITZ, JM ;
MOTL, ML .
NEUROPADIATRIE, 1971, 3 (01) :46-&
[4]   EPIDEMIOLOGY OF DELANGE,C-SYNDROME [J].
BECK, B .
ACTA PAEDIATRICA SCANDINAVICA, 1976, 65 (05) :631-638
[5]   FAMILIAL OCCURRENCE OF CORNELIA-DELANGES SYNDROME [J].
BECK, B .
ACTA PAEDIATRICA SCANDINAVICA, 1974, 63 (02) :225-231
[6]   CHROMOSOMES IN THE CORNELIA-DE-LANGE SYNDROME [J].
BECK, B ;
MIKKELSEN, M .
HUMAN GENETICS, 1981, 59 (04) :271-276
[7]  
BERATIS N G, 1971, Clinical Genetics, V2, P170
[8]  
BERG JM, 1970, DELANGE SYNDROME
[9]  
Borghi A, 1954, ACTA GENET MED GEMEL, V3, P365, DOI 10.1017/S1120962300021223
[10]  
Brachmann W., 1916, JB KINDERHEILK PHYS, V84, P225