J Korean Pediatr Soc.  2001 Apr;44(4):443-449.

Clinical Characteristics of Williams Syndrome

Affiliations
  • 1Department of Pediatrics, College of Medicine, Seoul National University, Seoul, Korea.

Abstract

PURPOSE
Williams syndrome(WS) is an autosomal dominant disorder resulting from a submicroscopic deletion of contiguous genes on the long arm of chromosome 7. We evaluated the physical, neurodevelopmental, and behavioral characteristics of children and adults with WS confirmed by fluorescence in situ hybridization.
METHODS
The clinically suspicious twelve cases with cardiac anomaly were confirmed as WS with fluorescence in situ hybridization(FISH) using the bacterial artificial chromosome clone 244H3, which has the genomic DNA sequence of elastin, as a probe. The neonatal history, facial features, associated anomaly including heart disease, neurological and behavioral characteristics were reviewed.
RESULTS
During the first year, infants with WS showed irritability(83%), vomiting, failure to thrive(58%), and feeding problems(50%). Inguinal and umbilical hernias were common(67%). The associated cardiac anomalies were supravalvular aortic stenosis(83%), most commonly and peripheral pulmonary stenosis(25%) and coarctatin of aorta(8%). The facial findings were periorbital swelling(100%), full and drooping cheek, thick lips, open wide mouth, full nasal tip(83%). Abnormal facial appearance became more striking during childhood and then more coarse by adolescence. Walking alone occurred at an average age of 24 months. Average I.Q. of about 62, with a range from 46 to 75(62+/-12) was recorded. The perceptual, especially visuospatial and motor funtions were more impaired than verbal performance. Distractibility, poor concentration and talk ativeness were very common. Aggressive behaviour was less common.
CONCLUSION
We conclude that molecular genetic analysis of 22q11 should be considered in patients with 1) supravalvular aortic stenosis or peripheral pulmonry stenosis, and 2) facial dysmorpholgy and 3) mental retardation with a friendly, outgoing personality, and 4) miserable infantile life with feeding problems such as vomiting and colic.

Keyword

Williams syndrome; Supravalvular aotic stenosis; Mental retardation

MeSH Terms

Adolescent
Adult
Aortic Stenosis, Supravalvular
Arm
Base Sequence
Cheek
Child
Chromosomes, Artificial, Bacterial
Chromosomes, Human, Pair 7
Clone Cells
Colic
Constriction, Pathologic
Elastin
Fluorescence
Heart Diseases
Hernia, Umbilical
Humans
In Situ Hybridization
Infant
Intellectual Disability
Lip
Molecular Biology
Mouth
Strikes, Employee
Vomiting
Walking
Williams Syndrome*
Elastin
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