SCARF syndrome

MONDO:0010728

A syndrome characterized by the association of skeletal abnormalities, cutis laxa, craniostenosis, ambiguous genitalia, psychomotor retardation and facial abnormalities. So far, it has been described in two males (maternal first cousins). The mode of inheritance was suggested to be X-linked recessive.

Also known as: SCARF syndrome, skeletal abnormalities, cutis laxa, craniostenosis, ambiguous genitalia, retardation, and Facial abnormalities

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

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↑ Syndromic disease (7133)

Including sub-types (0) Tagged with SCARF syndrome (0)

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