Prognosis and clinical characteristics of patients with 3β-hydroxy-Δ5-C27-steroid dehydrogenase deficiency diagnosed in childhood: A systematic review of the literature

OBJECTIVES: 3β-hydroxy-Δ5-C27-steroid dehydrogenase deficiency is a rare autosomal recessive condition. So far fewer than 100 cases have been reported and the factors affecting the prognosis are not yet established. The objective of this study is to explore a possible prediction of the outcome of th...

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Detalles Bibliográficos
Autores principales: Zhang, Yuan, Yang, Chun-Feng, Wang, Wen-Zhen, Cheng, Yong-Kang, Sheng, Chu-Qiao, Li, Yu-Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
4500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282059/
https://www.ncbi.nlm.nih.gov/pubmed/35363177
http://dx.doi.org/10.1097/MD.0000000000028834

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282059/
https://www.ncbi.nlm.nih.gov/pubmed/35363177
http://dx.doi.org/10.1097/MD.0000000000028834

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