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CHILD syndrome
rareCHILD 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.
- Identifiers
- MONDO:0010621 OMIM:308050Orphanet:139
- Causal genes
- NSDHL
- Part of
- X-linked ichthyosis syndromeBone benign neoplasmChondrodysplasia punctataHereditary disorder of connective tissueHereditary skin disorderMelanocytic nevusMultiple congenital anomalies/dysmorphic syndrome without intellectual disabilitySterol biosynthesis disorderSyndromic dyslipidemia
- Also known as
- child nevus · CHILD syndrome, X-linked dominant · congenital hemidysplasia with ichthyosiform nevus and limb defects · Ichthyosis, CHILD Syndrome
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