/CHILD syndrome

CHILD syndrome

Rare Disease

MONDO:0010621

Also Known As

CHILD syndromeCHILD syndrome, X-linked dominantIchthyosis, CHILD Syndromechild nevuschild syndromecongenital hemidysplasia with ichthyosiform nevus and limbs defectscongenital hemidysplasia with ichthyosiform erythroderma and limb defectscongenital hemidysplasia with ichthyosiform nevus and limb defectsichthyosiform erythroderma, unilateral, with ipsilateral malformations, especially absence deformity of limbsichthyosis, child syndrome

Definition

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.