A case of congenital goiter with congenital hypothyroidism due to organification defect
Journal of the Korean Pediatric Society
;
: 1002-1008, 1993.
Artigo
em Coreano
| WPRIM
| ID: wpr-39433
ABSTRACT
We experienced a case of congenital goiter with congenital hypothyroidism in 45 day-old male, who complained of respiratory difficulty and anterior neck mass. After admission, he was diagnosed congenital hypothyroidism by the clinical manifestations and laboratory tests including biochemistry, radioimmunoassay, radioisotope study, perchlorate discharge test, and bone radiography. We obtained positive finding at the perchlorate discharge test and found that his congenital goiter with congenital hypothyroidism was manifested by organification defect. We started treatment with L-thyroxine orally at 6th hospital day. The case was presented with brief review of literatures.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Tiroxina
/
Bioquímica
/
Radioimunoensaio
/
Radiografia
/
Hipotireoidismo Congênito
/
Bócio
/
Pescoço
Tipo de estudo:
Estudo diagnóstico
Limite:
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Journal of the Korean Pediatric Society
Ano de publicação:
1993
Tipo de documento:
Artigo
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