A familial case of Kallmann syndrome: novel variants in ANOS1 and GNRHR genes
ABSTRACT Kallmann syndrome (KS) is a rare genetic disorder characterized by hypogonadotropic hypogonadism and anosmia or hyposmia, stemming from the defective migration of GnRH and olfactory neurons during embryogenesis. This study investigated a multigenerational family with KS, identifying novel m...
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| Principais autores: | , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Sociedade Brasileira de Endocrinologia e Metabologia
2025-11-01
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| Serier: | Archives of Endocrinology and Metabolism |
| Fag: | |
| Online adgang: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972025000601500&lng=en&tlng=en |
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