Congenital adrenal hyperplasia due to 21-hydroxylase deficiency

precocious puberty. Patients and Methods: Thirty three patients with classic 21 hydroxylase deficiency (14 SW and 19 SV CAH) enrolled in the study. They were assessed and followed up for growth and developmental characteristics .All patients were karyotyped and sex was determined,…

Non-classical congenital adrenal hyperplasia or NCAH is a disorder that affects both men and women from late childhood through the rest of their lives. Compared to its sister form, classical congenital adrenal hyperplasia, it is non-life threatening. The Mayo Clinic, a service that gives people medical information and helps set up doctor appointments, defines NCAH as “a collection of genetic conditions that limit your adrenal glands' ability to make certain vital hormones.” These vital hormones…

Non-classical adrenal hyperplasia or NCAH is a disorder that affects both men and women from late childhood through the rest of their lives. Compared to its sister form, classical congenital adrenal hyperplasia, it is non-life threatening. The Mayo Clinic, a service that gives people medical information and helps set up doctor appointments, defines NCAH as “a collection of genetic conditions that limit your adrenal glands' ability to make certain vital hormones.” These vital hormones include,…