Literature DB >> 10360400

Microdeletion of chromosome sub-band 2q37.3 in two patients with abnormal situs viscerum.

K S Reddy1, D Flannery, R J Farrer.   

Abstract

We report on two cases of microdeletion of chromosome sub-band 2q37.3 with abnormal situs viscerum. The first patient had dextrocardia, duodenal and jejunal atresia, and an abdominal hernia. The liver was in the left upper quadrant, stomach in the right upper quadrant. In contrast anema the ascending colon was in the left, and descending colon on the right, with an area of atresia in the mid-jejunum. The second patient had malrotation and malposition of large and small bowel, with most of the bowels positioned above the liver and spleen. There was incomplete rotation of the cecum. The right kidney was malrotated and mal-positioned. The finding of 2q37.3 deletion in both patients implies that a locus or loci involved in the development of normal body situs lies within this chromosome region. Molecular cytogenetic evaluation for a possible 2q37.3 deletion should be considered in patients with abnormal situs viscerum.

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Year:  1999        PMID: 10360400     DOI: 10.1002/(sici)1096-8628(19990611)84:5<460::aid-ajmg10>3.0.co;2-l

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  5 in total

1.  A genome-wide scan for genes involved in primary vesicoureteric reflux.

Authors:  H Kelly; C M Molony; J M Darlow; M E Pirker; A Yoneda; A J Green; P Puri; D E Barton
Journal:  J Med Genet       Date:  2007-07-27       Impact factor: 6.318

Review 2.  Genetic factors in congenital diaphragmatic hernia.

Authors:  A M Holder; M Klaassens; D Tibboel; A de Klein; B Lee; D A Scott
Journal:  Am J Hum Genet       Date:  2007-04-04       Impact factor: 11.025

3.  Split cord malformation and situs inversus totalis: case report and review of the literature.

Authors:  R Shane Tubbs; John C Wellons; W Jerry Oakes
Journal:  Childs Nerv Syst       Date:  2004-01-23       Impact factor: 1.475

4.  Phenotypic variant of Brachydactyly-mental retardation syndrome in a family with an inherited interstitial 2q37.3 microdeletion including HDAC4.

Authors:  Pablo Villavicencio-Lorini; Eva Klopocki; Marc Trimborn; Randi Koll; Stefan Mundlos; Denise Horn
Journal:  Eur J Hum Genet       Date:  2012-11-28       Impact factor: 4.246

5.  Split cord malformation and situs inversus totalis: case report and review of the literature.

Authors:  R Shane Tubbs; John C Wellons; W Jerry Oakes
Journal:  Childs Nerv Syst       Date:  2003-11-26       Impact factor: 1.475

  5 in total

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