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A Case of Raine Syndrome
Article in Korean | WPRIM (Western Pacific) | ID: wpr-32027
Responsible library: WPRO
ABSTRACT
Raine syndrome was described as an unknown syndrome in 1989. It is characterized by severe craniofacial anomalies with microcephaly, hypoplastic nose, depressed nasal bridge, exophthamos/protosis, gum hypertrophy, cleft palate, low-set ears, small mandible, narrow chest, wide cranial sutures and choanal atresia or stenosis, by generalized osteosclerosis with subperiosteal thickening of ribs, clavicles and diaphysis of long bones, and by intracranial calcifications in the particularly periventricular area. It undergoes an autosomal recessive inheritance. Twelve cases of Raine syndrome have been reported in the literature. However, a case of Raine syndrome in Korea has not been reported yet. Therefore, we describe a female newborn with Raine syndrome with a brief review of the literatures.
Subject(s)

Full text: Available Database: WPRIM (Western Pacific) Limits: Female / Humans / Infant, Newborn Language: Korean Journal: Journal of the Korean Pediatric Society Year: 2003 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Limits: Female / Humans / Infant, Newborn Language: Korean Journal: Journal of the Korean Pediatric Society Year: 2003 Document type: Article
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