Multidisciplinary team management of 46,XY 17α-hydroxylase deficiency: a case report and literature review

BACKGROUND: We report here a case study of 17α-hydroxylase deficiency in a phenotypic girl with male karyotype (46,XY). We also review the relevant literature to deepen our understanding of the disease, reduce the rate of missed diagnosis, and emphasize that holistic management of this disease requi...

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Detalles Bibliográficos
Autores principales: Zhou, Yang, Xue, Xue, Shi, Panpan, Lu, Qinrui, Lv, Shulan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8165845/
https://www.ncbi.nlm.nih.gov/pubmed/33761789
http://dx.doi.org/10.1177/0300060521993965

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8165845/
https://www.ncbi.nlm.nih.gov/pubmed/33761789
http://dx.doi.org/10.1177/0300060521993965

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