Literature DB >> 23566844

A new case of partial 14q31.3-qter trisomy due to maternal pericentric inversion.

Ilária Cristina Sgardioli1, Milena Simioni, Nilma Lúcia Viguetti-Campos, Joana Rosa Prota, Vera Lúcia Gil-da-Silva-Lopes.   

Abstract

Chromosome 14 is often involved in chromosome rearrangements, although pericentric inversions are rare. Here we report a mother carrying a pericentric inversion of chromosome 14, and her daughter with recombinant chromosome characterized by a partial distal 14q trisomy. Principal clinical findings of the child include facial anomalies, microcephaly, developmental delay, hypotonia and cardiac malformation. Her final karyotype was 46,XX,rec(14)dup(14q)inv(14)(p12q31)mat[20], arr 14q31.3qter(85,427,839-106,356,482)x3. This report brings new data about clinical features of partial 14q trisomy and molecular analysis enables the visualization of genes involved in the segment duplicated.
Copyright © 2013 Elsevier B.V. All rights reserved.

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Year:  2013        PMID: 23566844     DOI: 10.1016/j.gene.2013.03.115

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  3 in total

1.  Recombinant chromosome with partial 14 q trisomy due to maternal pericentric inversion.

Authors:  Hande Küçük Kurtulgan; Leyla Özer; Malik Ejder Yıldırım; Evrim Ünsal; Süleyman Aktuna; Volkan Baltacı; Nejmiye Akkuş; İlhan Sezgin
Journal:  Mol Cytogenet       Date:  2015-11-21       Impact factor: 2.009

2.  14q32.3-qter trisomic segment: a case report and literature review.

Authors:  Nicoletta Villa; Agnese Scatigno; Serena Redaelli; Donatella Conconi; Paola Cianci; Clotilde Farina; Chiara Fossati; Leda Dalprà; Silvia Maitz; Angelo Selicorni
Journal:  Mol Cytogenet       Date:  2016-08-05       Impact factor: 2.009

Review 3.  A Recurrent De Novo Terminal Duplication of 14q32 in Korean Siblings Associated with Developmental Delay and Intellectual Disability, Growth Retardation, Facial Dysmorphism, and Cerebral Infarction: A Case Report and Literature Review.

Authors:  Ji Yoon Han; Joonhong Park
Journal:  Genes (Basel)       Date:  2021-09-07       Impact factor: 4.096

  3 in total

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