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Unusual presentation of Kallmannn syndrome with contiguous gene deletion in three siblings of a family
We report the case of 3 brothers aged 34, 24, and 22 years, unmarried, who presented to our endocrinology clinic with absence of secondary sexual characters. There was no such history in other siblings, but their maternal uncle had similar complaints. On examination, all 3 had pre-pubertal appearanc...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3603063/ https://ncbi.nlm.nih.gov/pubmed/23565415 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2230-8210.104077 |
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