A case report of pedigree of a homozygous mutation of the steroidogenic acute regulatory protein causing lipoid congenital adrenal hyperplasia
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference16 articles.
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4. Nonclassic congenital lipoid adrenal hyperplasia: a new disorder of the steroidogenic acute regulatory protein with very late presentation and normal male genitalia;Baker;J Clin Endocrinol Metab,2006
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1. Congenital lipoid adrenal hyperplasia in a Saudi infant;Endocrinology, Diabetes & Metabolism Case Reports;2022-09-01
2. Turner syndrome with positive SRY gene and non-classical congenital adrenal hyperplasia: A case report;World Journal of Clinical Cases;2021-04-06
3. Clinical and genetic characterization of congenital lipoid adrenal hyperplasia;Clinical Dysmorphology;2020-08-20
4. Long-term follow-up in a Chinese child with congenital lipoid adrenal hyperplasia due to a StAR gene mutation;BMC Endocrine Disorders;2018-11-06
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