Defective growth hormone secretion and hypogonadism in the new syndrome of congenital hypoparathyroidism, growth failure and dysmorphic features.
Indian J Pediatr
;
1996 Sep-Oct; 63(5): 679-82
Article
Dans Anglais
| IMSEAR
| ID: sea-83255
ABSTRACT
A child with extreme growth failure, dysmorphic features, hypoparathyroidism, and abnormal skeletal survey was studied. He was a product of first degree consaguineous marriage who had intrauterine growth retardation and presented at 14 days of age with hypocalcemic tetany with normal cardiovascular system and immune function. Endocrine evaluation after infancy revealed defective growth hormone (GH) secretion in 2 provocation tests and lack of clinical and testosterone response to human chorionic gonadotrophin (HCG) therapy.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
Sujet Principal:
Syndrome
/
Humains
/
Mâle
/
Nouveau-né
/
Enfant d'âge préscolaire
/
Études de suivi
/
Consanguinité
/
Malformations crâniofaciales
/
Hormone de croissance humaine
/
Nanisme
Type d'étude:
Étude observationnelle
/
Étude pronostique
langue:
Anglais
Texte intégral:
Indian J Pediatr
Année:
1996
Type:
Article
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