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Griffith CB et al. – The authors present three brothers with Simpson–Golabi–Behmel syndrome, all of which had cryptorchidism with one also having chordee of the penis, hypospadius, and penoscrotal transposition. While severe genital anomalies have been reported rarely in patients with Simpson–Golabi–Behmel syndrome, no individuals with such anomalies prior to this report had survived beyond the neonatal period.

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