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Biology of DSDs (4) Congenital Adrenal Hyperplasia
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Congenital Adrenal Hyperplasia, or CAH, is a group of sex development conditions which affect the adrenal glands and hormone production in both males and females. CAH occurs when genetic mutations cause the adrenal glands to produce excess sex hormones known as androgens.
Biology of DSDs playlist:
Transcripts, sources, and membership at:
References and additional reading:
[1] NIH. (2020). 21-hydroxylase deficiency. Genetics Home Reference, National Library of Medicine.
[2] LOCAH. (2018). The Intersex Masterpost. Medium.
[3] Witchel, S. (2018). Disorders of sex development. Best Practice and Research in Clinical Obstetrics and Gynecology, 48, 3.
[4] NIH. (2019). Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Genetic and Rare Diseases Information Center.
[5] Falhammar, H., et al. (2012). Clinical outcomes in the management of CAH. Endocrine, 41.
[6] Gidlof, S., et al. (2013). One hundred years of CAH in Sweden, a retrospective. Diab & Endocr, 1(1).
[7] Gliban, D., et al. (2014). Health related quality of life of children and adolescents with CAH in Brazil.
[8] Kovacs, J., et al. (2001). Lessons From 30 Years of Clinical Diagnosis and Treatment of CAH. Clinic Endoc.
[9] Nordenstrom, A., et al. (2010). Sexual function and surgical outcome in women with CAH. J Clin Endocrinol.
CAH support groups and foundations:
Biology of DSDs playlist:
Transcripts, sources, and membership at:
References and additional reading:
[1] NIH. (2020). 21-hydroxylase deficiency. Genetics Home Reference, National Library of Medicine.
[2] LOCAH. (2018). The Intersex Masterpost. Medium.
[3] Witchel, S. (2018). Disorders of sex development. Best Practice and Research in Clinical Obstetrics and Gynecology, 48, 3.
[4] NIH. (2019). Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Genetic and Rare Diseases Information Center.
[5] Falhammar, H., et al. (2012). Clinical outcomes in the management of CAH. Endocrine, 41.
[6] Gidlof, S., et al. (2013). One hundred years of CAH in Sweden, a retrospective. Diab & Endocr, 1(1).
[7] Gliban, D., et al. (2014). Health related quality of life of children and adolescents with CAH in Brazil.
[8] Kovacs, J., et al. (2001). Lessons From 30 Years of Clinical Diagnosis and Treatment of CAH. Clinic Endoc.
[9] Nordenstrom, A., et al. (2010). Sexual function and surgical outcome in women with CAH. J Clin Endocrinol.
CAH support groups and foundations:
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