A Case Report of 17α-Hydroxylase Deficiency in Two Saudi Siblings With Different Karyotyping

Souha Elabd; Ohoud Almohareb; Dania AlJaroudi; Ali Al Zahrani; Imad Brema; Souha El Abd; Ohoud Almohareb; Dania  AlJaroudi; Ali  Al Zahrani; Imad Brema

doi:10.7759/cureus.52191

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