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A Case of Marden-Walker Syndrome
Article in Ko | WPRIM | ID: wpr-113216
Responsible library: WPRO
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.
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Full text: 1 Database: WPRIM Main subject: Pneumonia, Aspiration / Blepharophimosis / Contracture / Arachnodactyly / Joints / Muscle Hypotonia Limits: Humans / Infant / Newborn Language: Ko Journal: Journal of the Korean Pediatric Society Year: 1999 Document type: Article
Full text: 1 Database: WPRIM Main subject: Pneumonia, Aspiration / Blepharophimosis / Contracture / Arachnodactyly / Joints / Muscle Hypotonia Limits: Humans / Infant / Newborn Language: Ko Journal: Journal of the Korean Pediatric Society Year: 1999 Document type: Article