Congenital adrenal hyperplasia in a child with 47, XYY: Case report

Author:

Close Sharron,Talboy Amy

Publisher

Elsevier BV

Subject

Pediatrics

Reference17 articles.

1. Increased basal and pulsatile secretion of FSH and LH in young men with 47,XXY or 46,XX karyotypes;Aksglaede;European Journal of Endocrinology,2008

2. Bone health should be an important concern in the care of patients affected by 21 hydroxylase deficiency;Bachelot;International Journal of Pediatric Endocrinoly,2010

3. 47,XYY syndrome: clinical phenotype and timing of ascertainment;Bardsley;Journal of Pediatrics,2013

4. Clinical aspects of infertile 47,XYY patients: a retrospective study;Boroujeni;Human Fertilityl (Camb),2019

5. Congenital adrenal hyperplasia-current insights in pathophysiology, diagnostics, and management;Claahsen-van der Grinten;Endocrine Reviews,2022

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