Hypogonadotropic hypogonadism in patients with multiple congenital defects
- PMID: 5317488
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Hypogonadotropic hypogonadism in patients with multiple congenital defects
Birth Defects Orig Artic Ser.
1971 May.
Abstract
Several syndromes have been reviewed in which hypogonadotropism is associated with multiple somatic and neurologic anomalies. A review of the literature indicates that these conditions demonstrate considerable clinical heterogeneity. In the several hypogonadotropic syndromes described to date autosomal and X-linked transmission have been implicated in the inheritance of the hypogonadism. The associated neurologic and somatic anomalies may segregate independent of the hypogonadism and in some instances may have a separate mode of transmission.
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