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X-linked recessive Kallmann syndrome: A case report
BACKGROUND: Kallmann syndrome (KS), also known as hypogonadotropic hypogonadism (HH) or olfactory-gonadal dysplasia, is a genetic condition in which the primary symptom is a failure to begin puberty or a failure to fully complete it. It occurs in both males and females and has the additional symptom...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Baishideng Publishing Group Inc
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9477064/ https://www.ncbi.nlm.nih.gov/pubmed/36157645 http://dx.doi.org/10.12998/wjcc.v10.i25.8990 |