دورية أكاديمية

Structural Chromosome Abnormalities Associated with Obesity: Report of Four New subjects and Review of Literature.

التفاصيل البيبلوغرافية
العنوان: Structural Chromosome Abnormalities Associated with Obesity: Report of Four New subjects and Review of Literature.
المؤلفون: Dasouki MJ; Departments of Pediatrics and Internal Medicine, Kansas University Medical Center, Kansas City, Kansas, USA., Youngs EL, Hovanes K
المصدر: Current genomics [Curr Genomics] 2011 May; Vol. 12 (3), pp. 190-203.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Bentham Science Publishers Country of Publication: United Arab Emirates NLM ID: 100960527 Publication Model: Print Cited Medium: Internet ISSN: 1875-5488 (Electronic) Linking ISSN: 13892029 NLM ISO Abbreviation: Curr Genomics Subsets: PubMed not MEDLINE
أسماء مطبوعة: Publication: Saif Zone, Sharjah, U.A.E. : Bentham Science Publishers
Original Publication: Hilversum, Netherlands ; Boca Raton, FL : Bentham Science Publishers, c2000-
مستخلص: Obesity in humans is a complex polygenic trait with high inter-individual heritability estimated at 40-70%. Candidate gene, DNA linkage and genome-wide association studies (GWAS) have allowed for the identification of a large set of genes and genomic regions associated with obesity. Structural chromosome abnormalities usually result in congenital anomalies, growth retardation and developmental delay. Occasionally, they are associated with hyperphagia and obesity rather than growth delay. We report four new individuals with structural chromosome abnormalities involving 10q22.3-23.2, 16p11.2 and Xq27.1-q28 chromosomal regions with early childhood obesity and developmental delay. We also searched and summarized the literature for structural chromosome abnormalities reported in association with childhood obesity.
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فهرسة مساهمة: Keywords: CNV.; Obesity; aCGH; chromosome; deletion; duplication; fluorescent in situ hybridization; translocation
تواريخ الأحداث: Date Created: 20111102 Date Completed: 20111110 Latest Revision: 20211020
رمز التحديث: 20221213
مُعرف محوري في PubMed: PMC3137004
DOI: 10.2174/138920211795677930
PMID: 22043167
قاعدة البيانات: MEDLINE
الوصف
تدمد:1875-5488
DOI:10.2174/138920211795677930