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Up to: Hereditary disorder of connective tissue · Hereditary skin disorder · Multiple congenital anomalies/dysmorphic syndrome without intellectual disability · Melanocytic nevus · Syndromic dyslipidemia · Bone benign neoplasm · Sterol biosynthesis disorder · Chondrodysplasia punctata · X-linked ichthyosis syndrome
CHILD syndrome
CHILD syndrome (Congenital Hemidysplasia with Ichthyosiform nevus and Limb Defects, CS) is an X-linked dominant genodermatosis characterized by unilateral inflammatory and scaling skin lesions with ipsilateral visceral and limb anomalies.
This condition has no sub-types.