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We have experienced three cases of female pseudohermaphroditism with congenital adrenal hyperplasia.
First case was salt-losing type and the other two cases were non salt-losing type. First patient, 2 months old female infant, was admitted to hospital because of vomiting, diarrhea, dehydration and ambiguous sex. In electrolyte study, she had hyponatremia and hyperkalemia. The other two cases, 2 Years 10 Months... |
