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Kallmann syndrome |
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Kallmann syndrome Hypogonadotropic hypogonadism A condition with a highly variable hereditary pattern, characterized by 2º hypogonadism Clinical Delayed puberty, micropenis, eunuchoid features, cryptorchidism, cleft lip and palate,
unilateral renal agenesis, horseshoe kidney, nerve deafness and hearing loss, color blindness, skeletal defects; synkinesia, spatial attention defects, spastic paraplegia, cerebellar dysfunction, horizontal nystagmus, pes cavus, mental retardation
Management Androgens; gonadotropins or LHRH for spermatogenesis. See Kalig-1. How to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit webmaster's page for free fun content. |
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There was tragedy even in Jimmy Scott's birth: He had Kallman's Syndrome, an hereditary, hormonal deficiency that arrested his growth, and as an adult, his voice and his appearance caused many to mistake him often for a woman. |
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