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PedAM

Pediatric Disease Annotations & Medicines




Disease n syndrome
Phenotype C0020619|hypogonadism
Sentences 8
PubMedID- 24083166 Anecdotal cases of reversal of hypogonadotropic hypogonadism in patients with kallmann syndrome have been reported.
PubMedID- 19489874 Objective: congenital hypogonadotropic hypogonadism with anosmia (kallmann syndrome) or with normal sense of smell is a heterogeneous genetic disorder caused by defects in the synthesis, secretion and action of gonadotrophin-releasing hormone (gnrh).
PubMedID- 21838873 It is well known that steinert's syndrome is closely related to some endocrine diseases, such as diabetes mellitus, insulin resistance, thyroidal diseases, adrenal insufficiency, hypogonadotropic hypogonadism and components of men syndromes [16-19].
PubMedID- 21836337 Bardet-biedl and laurence-moon syndromes are associated with mental retardation, hypogonadism, polydactyly and obesity.
PubMedID- 25131486 [micropump infusion of gonadorelin in the treatment of hypogonadotropic hypogonadism in patients with pituitary stalk interruption syndrome: cases analysis and literature review].
PubMedID- 23082007 Ica due to olfactory bulb agenesis and associated to hypogonadotropic hypogonadism defines kallmann syndrome (ks), in which several gene defects have been described.
PubMedID- 25559402 Context: a heterozygous de novo c.1228g>a mutation (e410k) in the tubb3 gene encoding the neuronal-specific beta-tubulin isotype 3 (tubb3) causes the tubb3 e410k syndrome characterized by congenital fibrosis of the extraocular muscles (cfeom), facial weakness, intellectual and social disabilities, and kallmann syndrome (anosmia with hypogonadotropic hypogonadism).
PubMedID- 25056118 At the other end of the spectrum, hyperleptinemia may play a role in hypogonadism associated with obesity, polycystic ovarian syndrome, and type 2 diabetes.

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