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PedAM

Pediatric Disease Annotations & Medicines




Disease cryptorchidism
Phenotype C0020619|hypogonadism
Sentences 2
PubMedID- 26160035 We present a case of 49,xxxxy sex polysomy, who shares a number of characteristics of the other 176 patients cases described in the literature, namely, hypogonadism with cryptorchidism, facial dysmorphism, musculoskeletal and cardiac malformations, and mental retardation seriously affecting language skills.
PubMedID- 22008714 hypogonadism with genital hypoplasia (cryptorchidism, scrotal or clitoral hypoplasia) can be identified in the newborn period.

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