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Article in Korean | WPRIM (Western Pacific) | ID: wpr-113216

ABSTRACT

Marden-Walder syndrome is characterized by a mask-like face, blepharophimosis, joint contractures, and psychometer retardation. We report a newborn infant with the clinical features of the syndrome. He was diagnosed with clinical findings of mask-like face, blepharophimosis, micrognathia, camptodactyly, arachnodactyly, multiple contractures, and hypotonia. The infant died of aspiration pneumonia at 5 months. A brief review of related literature is also presented.


Subject(s)
Humans , Infant , Infant, Newborn , Arachnodactyly , Blepharophimosis , Contracture , Joints , Muscle Hypotonia , Pneumonia, Aspiration
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