Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome

MONDO:0016386

This syndrome is characterized by the association of hypogonadotropic hypogonadism (with primary amenorrhea and lack of secondary sexual development) and retinitis pigmentosa. It has been described in two sisters born to nonconsanguineous parents.

Also known as: Chang-Davidson-Carlson syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome itself.

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↑ Syndromic disease (7158) ↑ Congenital hypogonadotropic hypogonadism (83)

Including sub-types (0) Tagged with Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome (0)

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