De Sanctis-Cacchione syndrome

MONDO:0010217

A rare autosomal recessive inherited syndrome. It is characterized by xeroderma pigmentosum, mental retardation, dwarfism, hypogonadism, and neurologic abnormalities.

Also known as: De Sanctis Cacchione Syndrome, de Sanctis-Cacchione syndrome, xerodermic idiocy

0 clinical trials for this condition and its sub-types, 0 tagged with De Sanctis-Cacchione syndrome itself.

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↑ Hereditary disease (18187) ↑ Syndromic disease (7133)

Including sub-types (0) Tagged with De Sanctis-Cacchione syndrome (0)

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