Literature DB >> 2692511

Duplication 7p de novo and literature review.

K Zerres1, G Schwanitz, K Gellissen, L Schroers, R Sohler.   

Abstract

We report on a boy with duplication of the short arm of chromosome 7 (karyotype 46,XY, dup (7) (p11.2----pter), QFQ, GTG, RBA). The boy showed delayed closure of fontanels, reduced eyebrows, short nose with low and broad nasal bridge, small upper and prominent full lower lips, severe delay of speech development. Comparison with the phenotype of 15 reported cases from the literature in relation to the extent of the duplicated segment did not show a clear phenotype/karyotype correlation.

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Year:  1989        PMID: 2692511

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


  4 in total

1.  A malformed child with a recombinant chromosome 7, rec(7) dup p, derived from a maternal pericentric inversion inv(7)(p15q36).

Authors:  A Delicado; E Escribano; I Lopez Pajares; A Diaz de Bustamante; S Carrasco
Journal:  J Med Genet       Date:  1991-02       Impact factor: 6.318

Review 2.  Cardiac malformation of partial trisomy 7p/monosomy 18p and partial trisomy 18p/monosomy 7p in siblings as a result of reciprocal unbalanced malsegregation--and review of the literature.

Authors:  Beate Schmidt; Floris Udink ten Cate; Michael Weiss; Udo Koehler
Journal:  Eur J Pediatr       Date:  2012-07       Impact factor: 3.183

3.  Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome.

Authors:  D Monk; E L Wakeling; V Proud; M Hitchins; S N Abu-Amero; P Stanier; M A Preece; G E Moore
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

4.  Intrachromosomal triplication of distal 7p.

Authors:  H Rivera; L Bobadilla; A Rolon; J Kunz; J A Crolla
Journal:  J Med Genet       Date:  1998-01       Impact factor: 6.318

  4 in total

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