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Congenital hemidysplasia with ichthyosiform nevus and limb defects (CHILD) syndrome is an X‐linked autosomal dominant disorder characterized by unilateral congenital hemidysplasia with ichthyosiform erythroderma and ipsilateral limb defects caused by a mutation in the gene encoding NAD[P]H steroid dehydrogenase‐like protein (NSDHL) at Xq28. The histopathologic hallmark of skin lesions in CHILD syndrome...
A meta‐analysis was conducted to evaluate the efficacy of propranolol in the treatment of infantile hemangiomas (IHs) in Chinese infants. A statistically significant difference was found between infants treated using propranolol and those treated using corticosteroids (p < 0.001). The total effect pooled from 26 single‐arm studies using meta‐analysis of propranolol on IHs in Chinese infants was...
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