Clinical and Experimental Pediatrics

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All issues > Volume 31(3); 1988

Original Article
J Korean Pediatr Soc. 1988;31(3):370-374. Published online March 31, 1988.
A Case of 18P-Syndrome with Frequent Intection.
Ellen A Kim1, Jong Sung Eum1, Hee Ju Kim1, Sung Ill Ahn1, Kyung Yu Park2
1Department of Pediatrics, Seoul Eul-Ji General Hospital
2Department of Otolaryngology, Seoul Eul-Ji General Hospital
Received: November 28, 1987;
Abstract
We herein reported a case of newborn with round face, low nasal bridge, micrognathia, down turning comers of mouth, large protruding ears, high arched palate with webbed short neck: This odd looking newborn was confirmed to have deltion of short arm of chromosome 18 (18P- syndrome). Frequent episodes of pneumonia developed until recently at 6 months of age. The cause of this frequent infection is uncertain but possibility of deficiency of secretory IgA was considered.

Keywords :18P- syndrome, Frequent infection.

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