Editorial: The etiology of thyroid dysgenesis - Still an enigma after all these years

被引:24
作者
Brown, RS [1 ]
Demmer, LA [1 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Pediat, Worcester, MA 01655 USA
关键词
D O I
10.1210/jc.2002-021092
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:4069 / 4071
页数:3
相关论文
共 20 条
[1]   Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid gland [J].
Abramowicz, MJ ;
Duprez, L ;
Parma, J ;
Vassart, G ;
Heinrichs, C .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (12) :3018-3024
[2]  
AHLBORN BE, 1997, HUM GENET, V99, P86
[3]   Mutations of the human thyrotropin receptor gene causing thyroid hypoplasia and persistent congenital hypothyroidism [J].
Biebermann, H ;
Schoneberg, T ;
Krude, H ;
Schultz, G ;
Gudermann, T ;
Gruters, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (10) :3471-3480
[4]   Influence of timing and dose of thyroid hormone replacement on development in infants with congenital hypothyroidism [J].
Bongers-Schokking, JJ ;
Koot, HM ;
Wiersma, D ;
Verkerk, PH ;
Keizer-Schrama, SMPFD .
JOURNAL OF PEDIATRICS, 2000, 136 (03) :292-297
[5]   Incidence of transient congenital hypothyroidism due to maternal thyrotropin receptor-blocking antibodies in over one million babies [J].
Brown, RS ;
Bellisario, RL ;
Botero, D ;
Fournier, L ;
Abrams, CAL ;
Cowger, ML ;
David, R ;
Fort, P ;
Richman, RA .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (03) :1147-1151
[6]   Developmental regulation of thyrotropin receptor gene expression in the fetal and neonatal rat thyroid: Relation to thyroid morphology and to thyroid-specific gene expression [J].
Brown, RS ;
Shalhoub, V ;
Coulter, S ;
Alex, S ;
Joris, I ;
De Vito, W ;
Lian, J ;
Stein, GS .
ENDOCRINOLOGY, 2000, 141 (01) :340-345
[7]   Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia [J].
Clifton-Bligh, RJ ;
Wentworth, JM ;
Heinz, P ;
Crisp, MS ;
John, R ;
Lazarus, JH ;
Ludgate, M ;
Chatterjee, VK .
NATURE GENETICS, 1998, 19 (04) :399-401
[8]  
COUVREUR J, 1991, ANN PEDIATR-PARIS, V38, P63
[9]   Deletion of thyroid transcription factor-1 gene in an infant with neonatal thyroid dysfunction and respiratory failure [J].
Devriendt, K ;
Vanhole, C ;
Matthijs, G ;
de Zegher, F .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (18) :1317-1318
[10]  
DUSSAULT JH, 1973, UNION MED CAN, V102, P2062