Literature DB >> 623059

Trisomy for the distal end of the short arm of chromosome 3: a syndrome.

J J Yunis.   

Abstract

We report a patient with a chromosomal syndrome involving trisomy for the distal three-fifths of the short arm of chromosome 3. The major clinical featues include bilateral temporal indentation, prominent cheeks, a long and prominent philtrum, protruding middle portion of the upper lip, penile hypoplasia, and an increased number of whorls on digits.

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Mesh:

Year:  1978        PMID: 623059     DOI: 10.1001/archpedi.1978.02120260032004

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  6 in total

1.  Secundum atrial septal defect associated with mitral valve cleft: report of a case with chromosomal syndrome of trisomy 3p.

Authors:  M Suzuki; S Ishikawa; A Ohtaki; K Sakata; O Kawashima; Y Otani; Y Morishita
Journal:  Surg Today       Date:  1996       Impact factor: 2.549

2.  Partial trisomy of the short arm of chromosome 3 (3p25 to 3pter). A distinct clinical entity.

Authors:  C Parloir; J P Fryns; H Van den Berghe
Journal:  Hum Genet       Date:  1979-04-05       Impact factor: 4.132

3.  Partial trisomy 3p in two siblings: clinical and pathological findings.

Authors:  N Van Regemorter; E Vamos; Y Gillerot; V Viteux; F Hayez; A Pardou; J Flament-Durand
Journal:  Eur J Pediatr       Date:  1983-10       Impact factor: 3.183

4.  Clinical and cytogenetic spectrum of duplication 3p.

Authors:  S Braga; A Schmidt
Journal:  Eur J Pediatr       Date:  1982-03       Impact factor: 3.183

5.  A complex three way translocation resulting in two sibs with partial trisomy 3p23----3pter.

Authors:  R Voss; E Gross-Kieselstein; H Hurvitz; J Dagan; E Kerem; J Zlotogora
Journal:  J Med Genet       Date:  1984-12       Impact factor: 6.318

6.  Chromosome 3p Inverted Duplication with Terminal Deletion: Second Postnatal Case Report with Additional Clinical Features.

Authors:  Jacquelyn D Riley; Catherine M Stefaniuk; Francine Erenberg; Angelika L Erwin; Lauren Palange; Caroline Astbury
Journal:  Case Rep Genet       Date:  2019-07-25
  6 in total

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