Disorders of sex development (DSD) 46.XY due to type 2 5-α reductase deficiency in three siblings: Case report from a low-resource setting

INTRODUCTION AND IMPORTANCE: Disorders of Sexual Development (DSD) is a rare autosomal recessive genetic condition significantly affecting patients' lives in various aspects, particularly psychosocially. Type 2 5-α reductase is a cause of DSD 46,XY. It is rare to find multiple DSDs in the same...

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Detalles Bibliográficos
Autores principales: Putri Susilo, Artha Falentin, Tjandraprawira, Kevin Dominique, Bayu, Patrick, Bayuaji, Hartanto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Case Series
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9577524/
https://www.ncbi.nlm.nih.gov/pubmed/36268297
http://dx.doi.org/10.1016/j.amsu.2022.104577

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9577524/
https://www.ncbi.nlm.nih.gov/pubmed/36268297
http://dx.doi.org/10.1016/j.amsu.2022.104577

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