CONGENITAL ADRENAL HYPERPLASIA;
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DOI:
https://doi.org/10.29309/TPMJ/2008.15.03.2840Keywords:
Congenital Adrenal Hyperplasia, 21-Hydroxylase deficiencyAbstract
Congenital Adrenal Hyperplasia is the most common cause of female intersex and is an autosomal
recessive disorder resulting in enzyme deficiency 21-hydroxylase. The case series describes three such cases that
are investigated and managed at Independent University Hospital Faisalabad.
