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kallmann syndrome		A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and olfactory nerve defects. It is characterized by congenital hypogonadotropic hypogonadism and anosmia, possibly with additional midline defects. It can be transmitted as an X-linked, an autosomal dominant, or an autosomal recessive trait. [ Articles | Books | Images | Discussion groups ]
Additional comments : See Also: Klinefelter Syndrome Hermaphroditism Pseudohermaphroditism

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