Kallmann's Syndrome Associasted with Slipped Capital Femoral Epiphysis / 대한내분비학회지
Journal of Korean Society of Endocrinology
;
: 318-323, 1996.
Artigo
em 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:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Cegueira
/
Hormônio Liberador de Gonadotropina
/
Síndrome de Kallmann
/
Criptorquidismo
/
Epífises
/
Colo do Fêmur
/
Escorregamento das Epífises Proximais do Fêmur
/
Córtex Olfatório
/
Lâmina de Crescimento
/
Cabeça
Limite:
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Journal of Korean Society of Endocrinology
Ano de publicação:
1996
Tipo de documento:
Artigo
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