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Syrian females with congenital adrenal hyperplasia: a case series إناث سوریات مصابات بتضخم الغدة الكظریة الخلقي: سلسلة حالات
Syrian females with congenital adrenal hyperplasia: a case series

إناث سوریات مصابات بتضخم الغدة الكظریة الخلقي: سلسلة حالات

 Title
Nada Dehneh, Rami Jarjour, Sahar Idelbi, Assad Alibrahem and Sahar Al Fahoum Authors
Journal of Medical Case Reports (vol. 16,1 371. 15 Oct. 2022)  Source title
1752-1947  ISSN 
Q3 Q 
 https://jmedicalcasereports.biomedcentral.com link

Background: One of the most common types of congenital adrenal hyperplasia is an autosomal recessive disorder with 21-hydroxylase deficiency. The classical form, defined by cortisol insufficiency, is accompanied by prenatal androgen excess causing variable masculinization degrees of external genitalia in babies with a 46, XX karyotype. Cases presentation: These five case reports highlight the management of Syrian females aged between 0 and 32 years with congenital adrenal hyperplasia. Two of the patients have been raised as males, while two had reconstructive surgery and one had hormonal therapy. Becoming mother was achieved by two patients Conclusion: The integrated treatment of females with classical congenital adrenal hyperplasia CAH, which includes appropriate surgical procedures and controlled hormonal therapy, gives these females the opportunity to live as they are, and perhaps as mothers in the future. .  .
ABSTRACT

 



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