A Chinese girl with delayed puberty due to 17α-hydroxylase deficiency: the diagnosis, treatment and monitoring approach

SUMMARY: 17α-hydroxylase deficiency (17α-OHD) is a rare form of congenital adrenal hyperplasia. We report the case of a teenage girl with 17α-OHD who presented with delayed puberty, hypergonadotropic hypogonadism and hypertension. We illustrate the clinical approach in workup, the subsequent managem...

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Detalles Bibliográficos
Autores principales: Yu, Geoffrey Chek Fei, Tay, Ming-kut, Chen, Sammy Pak-lam, Leung, Mei Tik Stella, Tung, Joanna Yuet-ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2023
Materias:
New Disease or Syndrome: Presentations/Diagnosis/Management
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563631/
https://www.ncbi.nlm.nih.gov/pubmed/37747283
http://dx.doi.org/10.1530/EDM-23-0047

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563631/
https://www.ncbi.nlm.nih.gov/pubmed/37747283
http://dx.doi.org/10.1530/EDM-23-0047

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