Trisomy of the short arm of chromosome 10.

Journal of medical genetics ·Vol. 12 ·No. 4 ·1975-12-00 ·Pages 412-4

Nakagome Y, Kobayashi H

Abstract

A case of a fetus with multiple malformations is described. The mother showed a 46,XX,rcp(10;22) (p11;p11) karyotype. Amniocentesis at the 16th week of gestation revealed that the male fetus had a der(22) chromosome--that is, he was trisomic for a large part of 10p (10pter leads to 10p11). Clinical findings of cases with 10p, 10q, and mosaic 10 trisomies are briefly reviewed.

MeSH Terms

Adult Chromosomes, Human, 19-20 Congenital Abnormalities/genetics Female Fetal Diseases/genetics Humans Male Pregnancy Translocation, Genetic Trisomy

Authors & Affiliations

2 authors, click to expand affiliations / ORCID

Nakagome Y

Kobayashi H

References (4)

4 references, click to expand

Trisomy 10 with mosaicism. A clinical and cytogenetic entity.
Jinrui Idengaku Zasshi. 1973 Sep;18(2):216-9 PMID: 4797432
[A case of multiple congenital anomalies with familial C-G translocation].
Jinrui Idengaku Zasshi. 1970 Mar;14(4):309-15 PMID: 5464693
[Multiple malformations in partial trisomy C (12) as manifestation of an inherited E-C (18/12) translocation].
Helv Paediatr Acta. 1967 Apr;22(1):41-53 PMID: 5585048
G-group chromosomes in satellite associations.
Cytogenet Cell Genet. 1973;12(5):336-41 PMID: 4131090

Article Info

Journal

Journal of medical genetics

Abbr.

J Med Genet

ISSN

0022-2593

DOI

10.1136/jmg.12.4.412

Published

1975-12-00

Pages

412-4

Language

English

Region

England

NLM ID

2985087R

PMCID

PMC1013323

Subset

External Links

PubMed source DOI: 10.1136/jmg.12.4.412 PMC Full Text View journal details

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Trisomy of the short arm of chromosome 10.

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