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PAUL SAENGER, ALLEN S. GOLDMAN, LENORE S. LEVINE, SIGRUN KORTH SCHUTZ, EDWARD C. MUECKE, MASUYUKI KATSUMATA, YALE DOBERNE, MARIA I. NEW, Prepubertal Diagnosis of Steroid 5α-Reductase Deficiency, The Journal of Clinical Endocrinology & Metabolism, Volume 46, Issue 4, 1 April 1978, Pages 627–634, https://doi.org/10.1210/jcem-46-4-627
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Abstract
The diagnosis of 5α-reductase deficiency was proven in two prepubertal patients with male pseudohermaphroditism (MPH). Both had a 46-XY karyotype and were reared as females; one child had been castrated in infancy. Clitoromegaly, urogenitalsinus, and short vaginal pouch were present in both; inguinal gonads were palpable in one.
The diagnosis was made biochemically by observing characteristic changes in five parameters: 1) abnormally high testosterone to dihydrotestosterone (T:DHT) ratio after hCG stimulation (35 and 53 vs. normal, 11 ± 3), 2) abnormally high 5β/5α-T metabolites in urine (8.1 and 6.0 vs. normal, <1), 3) deficient conversion of T to DHT during [3H]T infusion (0.3 and 0.4% vs. normal, 5.3 ± 3), 4) deficient conversion of [14C]T to 5α-reduced metabolitesby nongenital skin fibroblasts (2.2 and 1.9 pmol/μg DNA/nmol substrate vs. 68.4 ± 7.8 pmol/μg DNA/nmol substrate in normal controls), and 5) deficient conversion of [14C]T to DHT in genital skin slices.
The fact that this syndrome represents a defect in T metabolism rather than in T binding is demonstrated by the observation that binding of [3H]DHT to cytosol of skin fibroblasts was normal (4.2 dpm/μg DNA vs. normal male values of 3.7 ± 0.64).
Thus, the present report suggests that 5α-reductase deficiency can be diagnosed during childhood and even after castration by metabolic studies of nongenital skin fibroblasts and by determination of the conversion ratio of [3H]T to [3H]DHT in plasma.
