Literature DB >> 11343338

Unique case of trisomy 2p24.3-pter with no associated monosomy.

J A Roggenbuck1, J M Fink, N J Mendelsohn.   

Abstract

We report a 3-year-old girl with trisomy 2p24.3-pter who presented with marked psychomotor delay and dysmorphic features. This patient represents the only known case of trisomy 2p24.3-2pter that does not involve an associated functional monosomy. In contrast to recent reports highlighting the fatal or serious complications in patients described as having partial trisomy 2p, this patient does not have significant birth defects or life threatening medical problems. Notably, this patient does not have a neural tube defect (NTD), which has been attributed to a putative locus at 2p24 in other patients with a partial trisomy 2p. Copyright 2001 Wiley-Liss, Inc.

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Year:  2001        PMID: 11343338

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


  2 in total

1.  A Two-Month-Old Child with Vascular Ectasia: A Case Report Diagnosed by Molecular Karyotyping.

Authors:  Ozlem Tolu Kendir; Hayri Levent Yilmaz; Sevcan Bozdogan; Atıl Bisgin; Tugçe Celik; Ozgur Surmelioglu; Figen Doran
Journal:  J Pediatr Genet       Date:  2018-08-22

2.  Fetal Cystic Hygroma Associated with Terminal 2p25.1 Duplication and Terminal 3p25.3 Deletion: Cytogenetic, Fluorescent in Situ Hybridization and Microarray Familial Characterization of Two Different Chromosomal Structural Rearrangements.

Authors:  F Stipoljev; M Barbalic; M Logara; A Vicic; M Vulic; S Zekic Tomas; R Gjergja Juraski
Journal:  Balkan J Med Genet       Date:  2021-03-23       Impact factor: 0.519

  2 in total

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