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PMID: 3177451 Published · ppublish English Case Reports Journal Article

A new syndrome with mental retardation, short stature and an Xq duplication.

American journal of medical genetics ·Vol. 30 ·No. 1-2 ·1988-00-00 ·Pages 239-50

Thode A, Partington MW, Yip MY, Chapman C, Richardson VF, Turner G

Abstract

We describe a new X-linked syndrome of marked short stature, severe intellectual handicap and an unusual facial appearance. High resolution prometaphase banding showed affected males to have an X chromosome tandem duplication; their karyotypes were designated 46,dup(X) (q13.1-q21.1)Y. In carrier females the abnormal X chromosome was late replicating. To verify the duplication, gene dosage studies were performed using an enzyme assay and DNA techniques. Prenatal diagnosis is available for carrier females using chromosome analysis of amniocytes or chorionic villi.

MeSH Terms
Child Child, Preschool Chromosome Aberrations Female Genetic Linkage Growth Disorders/genetics Heterozygote Humans Intellectual Disability/genetics Male Multigene Family Pedigree Syndrome X Chromosome
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Thode A
Department of Medical Genetics, Prince of Wales Children's Hospital, Sydney, Australia.
Partington M W
Yip M Y
Chapman C
Richardson V F
Turner G
Article Info
Journal
American journal of medical genetics
Abbr.
Am J Med Genet
ISSN
0148-7299
Published
1988-00-00
Pages
239-50
Language
English
Region
United States
NLM ID
7708900
Subset
IM
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