Partial trisomy 10p and familial translocation t(7;10)(p22;p12).

Human genetics ·Vol. 35 ·No. 3 ·1977-03-14 ·Pages 353-6

Johnson G, Bachman R, Roed T, Riddervold P

Abstract

A girl with partial trisomy for the short arm of chromosome 10(p12leads to pter) due to mal chromosome segregation in the father 46,XY,t(7;10)(p22;p12) is described. The major abnormalities in this case are: mottled skin, mid-facial hypoplasia, low percentiles for weight, length, and head circumference, and club feet.

MeSH Terms

Abnormalities, Multiple/genetics Chromosome Aberrations Chromosomes, Human, 6-12 and X Female Humans Infant Phenotype Translocation, Genetic Trisomy

Authors & Affiliations

4 authors, click to expand affiliations / ORCID

Johnson G

Bachman R

Roed T

Riddervold P

References (3)

3 references, click to expand

Partial trisomy 10p.
Humangenetik. 1975 Sep 10;29(2):141-4 PMID: 1176136
Trisomy for the short arm of chromosome No. 10.
Clin Genet. 1974;6(5):408-15 PMID: 4434655
Brother and sister with trisomy 10p: a new syndrome.
Humangenetik. 1974;23(3):163-72 PMID: 4844639

Article Info

Journal

Human genetics

Abbr.

Hum Genet

ISSN

0340-6717

DOI

10.1007/BF00446626

Published

1977-03-14

Pages

353-6

Language

English

Region

Germany

NLM ID

7613873

Subset

External Links

PubMed source DOI: 10.1007/BF00446626 View journal details

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Partial trisomy 10p and familial translocation t(7;10)(p22;p12).

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