Clinical Characteristics and Genetic Analysis of Prader-Willi Syndrome.
- Author:
Ji Eun LEE
1
;
Kwang Bin MOON
;
Jong Hee HWANG
;
Eun Kyung KWON
;
Sun Hee KIM
;
Jong Won KIM
;
Dong Kyu JIN
Author Information
1. Department of Pediatrics, College of Medicine, Sungkyunkwan University, Seoul, Korea. jindk@smc.samsung.co.kr
- Publication Type:Original Article
- Keywords:
Prader-Willi syndrome;
Clinical feature;
Genetic analysis
- MeSH:
Birth Weight;
Chromosome Aberrations;
CpG Islands;
Cytogenetics;
Diagnosis;
Diagnostic Tests, Routine;
Humans;
In Situ Hybridization, Fluorescence;
Molecular Biology;
Muscle Hypotonia;
Pediatrics;
Polymerase Chain Reaction;
Prader-Willi Syndrome*;
Retrospective Studies;
snRNP Core Proteins;
Uniparental Disomy;
Weight Gain
- From:Journal of the Korean Pediatric Society
2002;45(9):1126-1133
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: Prader-Willi syndrome(PWS) is a complex disorder affecting multisystems with characteristic clinical features. Its genetic basis is an expression defect in the paternally derived chromosome 15q11-q13. We analyzed the clinical features and genetic basis of PWS patients for early detection and treatment. METHODS: We retrospectively studied 24 patients with PWS in Department of Pediatrics, Samsung Medical Center, from September 1997 to September 2001. We performed cytogenetic and molecular genetic techniques using high resolution GTG banding techniques, fluorescent in situ hybridization and methylation-specific PCR for CpG island of SNRPN gene region. RESULTS: The average birth weight of PWS patients was 2.67+/-0.47 kg and median age at diagnosis was 1.3 years. The average height and weight of PWS patients under one year at diagnostic time were located in a 3-10 percentile relatively, and a rapid weight gain was seen between two and six years. Feeding problems in infancy and neonatal hypotonia were the two most consistently positive major criteria in over 95% of the patients. In 18 of the 24 cases(75%), deletion of chromosome 15q11-q13 was demonstrated and one case among 18 had an unbalanced 14;15 translocation. In four cases without any cytogenetic abnormality, it may be considered as maternal uniparental disomy and the rest showed another findings. CONCLUSION: We suggest diagnostic testing for PWS in all infants/neonates with unexplained feeding problems and hypotonia. It is necessary for clinically suspicious patients to undergo an early genetic test. As the genetic basis of PWS was heterogenous and complex, further study is required.
