Greene S A, Symes E, Brook C G
Arch Dis Child. 1978 Sep;53(9):751-3. doi: 10.1136/adc.53.9.751.
An infant with male pseudohermaphroditism due to deficiency of 5-alpha-reductase is described, the elder of two affected male siblings. These patients, who come from Pakistan, are the first to be described outside America.
本文描述了一名因5-α还原酶缺乏导致男性假两性畸形的婴儿,他是两名受影响男性同胞中的年长者。这些来自巴基斯坦的患者是美国以外首次被描述的此类病例。