Home LiteratureArticle Details
PMID: 6713711 Published · ppublish English Case Reports Comparative Study Journal Article

Duplication or insertion in 15q11-13 associated with mental retardation-short stature and obesity-Prader-Willi or Cohen syndrome?

Clinical genetics ·Vol. 25 ·No. 4 ·1984-04-00 ·Pages 347-52

Fuhrmann-Rieger A, Köhler A, Fuhrmann W

Abstract

Difficulties of differential diagnosis between Prader-Willi Syndrome and Cohen Syndrome are demonstrated in a 12-year-old girl with obesity and mental retardation. Cytogenetic studies showed an apparently supernumerary band on chromosome 15 in the proximal region q11-13. Both parents have a normal karyotype. The aberrant chromosome was derived from an apparently normal paternal chromosome.

MeSH Terms
Abnormalities, Multiple/diagnosis,genetics Child Chromosome Aberrations Chromosomes, Human, 13-15 Diagnosis, Differential Female Humans Intellectual Disability/genetics Obesity/genetics Prader-Willi Syndrome/diagnosis,genetics
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Fuhrmann-Rieger A
Köhler A
Fuhrmann W
Article Info
Journal
Clinical genetics
Abbr.
Clin Genet
ISSN
0009-9163
Published
1984-04-00
Pages
347-52
Language
English
Region
Denmark
NLM ID
0253664
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com