Literature DB >> 434890

Familial partial trisomy of the long arm of chromosome 3 (3q).

C Fear, A Briggs.   

Abstract

A case of partial trisomy of the long arm of chromosome 3 (3q21 leads to qter) is described. The clinical findings are compared with those in 5 previously reported cases. There is hirsutism and characteristic facial dysmorphism, the common features of which are a square-shaped face, prominent nasal bridge, everted nostrils, hypertelorism, and palate abnormalities; occurring less often are abnormalities of vertebrae, thorax, and digits, or cardiovascular, urinogenital, and central nervous system. New features noted in this present case are absence of right eye from orbit and spina bifida. The spectrum of this syndrome is discussed, with possible relation to the degree of trisomy. The present case is the 6th to be reported with partial trisomy of the long arm of chromosome 3.

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Year:  1979        PMID: 434890      PMCID: PMC1545362          DOI: 10.1136/adc.54.2.135

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  4 in total

1.  A FAMILY APPARENTLY SHOWING TRANSMISSION OF A TRANSLOCATION BETWEEN CHROMOSOME 3 AND ONE OF THE 'X-6-12' OR 'C' GROUP.

Authors:  G CLARKE; A C STEVENSON; P DAVIES; C E WILLIAMS
Journal:  J Med Genet       Date:  1964-09       Impact factor: 6.318

2.  A case of partial trisomy 3q.

Authors:  H Chiyo; Y Kuroki; I Matsui; N Niitsu; Y Nakogome
Journal:  J Med Genet       Date:  1976-12       Impact factor: 6.318

3.  Precise identification of various chromosomal abnormalities.

Authors:  K Hirschhorn; M Lucas; I Wallace
Journal:  Ann Hum Genet       Date:  1973-04       Impact factor: 1.670

4.  [Familial translocation 3/22 MAT with partial trisomy 3q (author's transl)].

Authors:  G Schwanitz; R D Schmid; G Grosse; E Grahn-Liebe
Journal:  J Genet Hum       Date:  1977-06
  4 in total
  5 in total

Review 1.  A novel case of unilateral blepharophimosis syndrome and mental retardation associated with de novo trisomy for chromosome 3q.

Authors:  T Cai; D A Tagle; X Xia; P Yu; X X He; L Y Li; J H Xia
Journal:  J Med Genet       Date:  1997-09       Impact factor: 6.318

2.  Craniofacial dysmorphogenesis including cleft palate in mice with an insertional mutation in the discs large gene.

Authors:  G Caruana; A Bernstein
Journal:  Mol Cell Biol       Date:  2001-03       Impact factor: 4.272

Review 3.  Partial 3q duplication syndrome and assignment of D3S5 to 3q25-3q28.

Authors:  A J van Essen; K Kok; A van den Berg; B de Jong; F Stellink; A F Bos; H Scheffer; C H Buys
Journal:  Hum Genet       Date:  1991-06       Impact factor: 4.132

4.  Prenatally diagnosed partial trisomy 3q case with an omphalocele and less severe phenotype.

Authors:  Deniz Cemgil Arıkan; Ayhan Coşkun; Ilker Arıkan; Gürkan Kıran; Gülay Ceylaner
Journal:  J Turk Ger Gynecol Assoc       Date:  2010-12-01

Review 5.  Chromosome abnormalities and the genetics of congenital corneal opacification.

Authors:  A Mataftsi; L Islam; D Kelberman; J C Sowden; K K Nischal
Journal:  Mol Vis       Date:  2011-06-17       Impact factor: 2.367

  5 in total

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