Literature DB >> 16970040

Partial trisomy of long arm of chromosome 4 as a result of dir dup (4)(q27q31.3) de novo.

E Hubert1, A Sawicka, E Wasilewska, A T Midro.   

Abstract

The phenotype of a girl at age of 12 years with a partial trisomy 4q caused by unique direct duplication 4q27 --> q31.3 included the thick, broad and straight eyebrows, upward slanting palpebral fissures, a deep-set eyes, narrow bridge and long back of the nose, flattened philtrum columns, narrow of vermilion borders of both upper and lower lips, protrusion of maxillary alveolar processus and anterior teeth together with shortened and posteriorly situated mandible, malocclusion corresponding with II class of Angle and long fingers, narrowing towards distal phalanges has been described. Further investigations are needed to delineate the clinical spectrum of features essential for partial trisomy 4q.

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Mesh:

Year:  2006        PMID: 16970040

Source DB:  PubMed          Journal:  Genet Couns        ISSN: 1015-8146


  3 in total

1.  Recurrent 70.8 Mb 4q22.2q32.3 duplication due to ovarian germinal mosaicism.

Authors:  Lucie Tosca; Sophie Brisset; François M Petit; Laure Lecerf; Ghislaine Rousseau; Cécile Bas; Mireille Laroudie; Marie-Laure Maurin; Sylvie Tapia; Olivier Picone; Sophie Prevot; Michel Goossens; Philippe Labrune; Gérard Tachdjian
Journal:  Eur J Hum Genet       Date:  2010-04-28       Impact factor: 4.246

2.  Case Report: Phenotype-Gene Correlation in a Case of Novel Tandem 4q Microduplication With Short Stature, Speech Delay and Microcephaly.

Authors:  Umm-Kulthum Ismail Umlai; Basma Haris; Khalid Hussain; Puthen Veettil Jithesh
Journal:  Front Endocrinol (Lausanne)       Date:  2022-02-03       Impact factor: 5.555

3.  Gain of chromosome 4qter and loss of 5pter: an unusual case with features of cri du chat syndrome.

Authors:  Frenny Sheth; Naresh Gohel; Thomas Liehr; Olakanmi Akinde; Manisha Desai; Olawaleye Adeteye; Jayesh Sheth
Journal:  Case Rep Genet       Date:  2012-12-20
  3 in total

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