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CHILD Syndrome


Rare variant of ichthyosiform erythroderma characterized by Congenital Hemidysplasia, unilateral Ichthyosiform erythroderma and Limb Defects. Although there is a sharp midline demarcation of a unilateral ichthyosiform erythroderma, some minor involvement of the opposite side may occur. Limb defects are ipsilateral to the ichthyosis, ranging in severity from hypoplasia of the fingers to complete agenesis of the extremity. Ipsilateral hypoplasia of other skeletal components may also occur, as well as other anomalies, including CNS, cardiovascular, renal, thyroid, and genitourinary.




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