Familial Glucocorticoid Deficiency Type 2: A Case Report - Case Report
Author:
Publisher
Galenos Yayinevi
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health
Link
http://cms.galenos.com.tr/FileIssue/1/376/article/122-125.pdf
Cited by 11 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Expanding the Phenotype of Congenital Glucocorticoid Deficiency: An Iranian Patient with Cholestasis due to Pathogenic Variants in the MC2R Gene;International Journal of Endocrinology;2024-01
2. Growth alterations in rare forms of primary adrenal insufficiency: a neglected issue in paediatric endocrinology;Endocrine;2022-10-30
3. A Novel Mutation in Melanocortin Receptor 2 and a Reported Mutation in Melanocortin Receptor 2 Accessory Protein: Three Chinese Cases with Familial Glucocorticoid Deficiency;Molecular Syndromology;2022-10-11
4. Adrenocorticotrophin;The Pituitary;2022
5. Adrenal Gland Signs;Endocrine Pathophysiology;2020
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