Congenital hypothyroidism and concomitant anomalies

被引:0
作者
Chao, T [1 ]
Wang, JR [1 ]
Hwang, BT [1 ]
机构
[1] VET GEN HOSP, DEPT PEDIAT, TAIPEI, TAIWAN
关键词
congenital hypothyroidism; congenital anomalies; neonatal screening;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To search for concomitant anomalies among babies with congenital hypothyroidism, 120 newborn babies with confirmed congenital hypothyroidism were studied at the Veterans General Hospital, Taipei, The incidence of concomitant anomalies was estimated to be 11.67% (14/120), Among these anomalies, cardiac and gastrointestinal systems were the most commonly involved, comprising 35.7% (5/14) and 28.6% (4/14) of all anomalies, respectively. The type (i.e. agenesis, ectopia or eutopic goiter) as well as the severity of hypothyroidism were analyzed between groups of babies with or without concomitant anomalies. No differences existed between the two groups of babies regarding these two aspects.
引用
收藏
页码:217 / 221
页数:5
相关论文
共 11 条
[1]   CONGENITAL-ANOMALIES ASSOCIATED WITH HYPOTHYROIDISM [J].
BAMFORTH, JS ;
HUGHES, I ;
LAZARUS, J ;
JOHN, R .
ARCHIVES OF DISEASE IN CHILDHOOD, 1986, 61 (06) :608-609
[2]   CONGENITAL-ANOMALIES ASSOCIATED WITH HYPOTHYROIDISM [J].
CHANOINE, JP ;
BOURDOUX, P ;
DELANGE, F .
ARCHIVES OF DISEASE IN CHILDHOOD, 1986, 61 (11) :1147-1147
[3]  
FERNHOFF PM, 1987, LANCET, V1, P490
[4]  
GOUJARD J, 1981, ARCH FR PEDIATR, V38, P875
[5]   SURVEY OF NEONATAL SCREENING FOR PRIMARY HYPOTHYROIDISM IN ENGLAND, WALES, AND NORTHERN-IRELAND 1982-4 [J].
GRANT, DB ;
SMITH, I .
BRITISH MEDICAL JOURNAL, 1988, 296 (6633) :1355-1358
[6]  
KLEIN RZ, 1988, J PEDIATR-US, V112, P244
[7]  
LAZARUS JH, 1988, LANCET, V2, P52
[8]  
NIEU DM, 1995, CHIN MED J TAIPEI, V56, P345
[9]   CONGENITAL HYPOTHYROIDISM - INCREASED INCIDENCE IN ASIAN FAMILIES [J].
ROSENTHAL, M ;
ADDISON, GM ;
PRICE, DA .
ARCHIVES OF DISEASE IN CHILDHOOD, 1988, 63 (07) :790-793
[10]   CONGENITAL-ANOMALIES CONCOMITANT WITH PERSISTENT PRIMARY CONGENITAL HYPOTHYROIDISM [J].
SIEBNER, R ;
MERLOB, P ;
KAISERMAN, I ;
SACK, J .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 44 (01) :57-60