Kallmann's Syndrome Associasted with Slipped Capital Femoral Epiphysis / 대한내분비학회지
Journal of Korean Society of Endocrinology
;
: 318-323, 1996.
Artículo
en Coreano
| WPRIM
| ID: wpr-765564
ABSTRACT
The Kallmanns syndrome is the most common form of isolated hypogonadotropic hypogonadism in which anosmia or hyposmia resulting from agenesis of hypoplasia of the olfactory lobes is associated with LHRH deficiency, This syndrome is genetically heterogeneous and can be trans-mitted as an X-linked, autosomal dominant or autosomal recessive trait. The hypogonadotropic hypogonadism results in absent or incomplete pubertal development and may be associated with anosmia or hyposmia, mid-line defect(color blindness, cleft-lip or
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Ceguera
/
Hormona Liberadora de Gonadotropina
/
Síndrome de Kallmann
/
Criptorquidismo
/
Epífisis
/
Cuello Femoral
/
Epífisis Desprendida de Cabeza Femoral
/
Corteza Olfatoria
/
Placa de Crecimiento
/
Cabeza
Límite:
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Journal of Korean Society of Endocrinology
Año:
1996
Tipo del documento:
Artículo
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