Literature DB >> 25944787

A familial 7q36.3 duplication associated with agenesis of the corpus callosum.

Keith Wong1, Randal Moldrich2, Matthew Hunter1,3, Matthew Edwards4, David Finlay5, Sheridan O'Donnell3, Tom MacDougall6, Nicole Bain7, Benjamin Kamien1,3.   

Abstract

Small chromosomal duplications involving 7q36.3 have rarely been reported. This clinical report describes four individuals from a three-generation family with agenesis of the corpus callosum (ACC) and a 0.73 Mb duplication of 7q36.3 detected by array CGH. The 7q36.3 duplication involves two genes: RNA Binding Motif Protein 33 (RBM33) and Sonic Hedgehog (SHH). Most affected family members had mild intellectual disability or borderline intellectual functioning, macrocephaly, a broad forehead, and widely spaced eyes. Two individuals had a Chiari type I malformation. This is the first family reported with ACC associated with a small duplication of these genes. While we cannot establish causation for the relationship between any single gene and the ACC in this family, there is a role for SHH in the formation of the corpus callosum through correct patterning and assembly of the commissural plate, and these data concur with vertebrate studies showing that a gain of SHH expands the facial primordium.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  Chiari malformation; RBM33; SHH; agenesis of the corpus callosum; chromosome 7q36.3; macrocephaly; sonic hedgehog

Mesh:

Substances:

Year:  2015        PMID: 25944787     DOI: 10.1002/ajmg.a.37143

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  4 in total

1.  Mutations in the sonic hedgehog pathway cause macrocephaly-associated conditions due to crosstalk to the PI3K/AKT/mTOR pathway.

Authors:  Steven D Klein; Dzung C Nguyen; Viraj Bhakta; Derek Wong; Vivian Y Chang; Tom B Davidson; Julian A Martinez-Agosto
Journal:  Am J Med Genet A       Date:  2019-10-22       Impact factor: 2.578

2.  Molecular characterization of a rare analphoid supernumerary marker chromosome derived from 7q35 → qter: a case report.

Authors:  Bárbara Marques; Cristina Ferreira; Filomena Brito; Sónia Pedro; Cristina Alves; Teresa Lourenço; Marta Amorim; Hildeberto Correia
Journal:  Mol Cytogenet       Date:  2016-11-25       Impact factor: 2.009

3.  De novo chromosome 7q36.1q36.2 triplication in a child with developmental delay, growth failure, distinctive facial features, and multiple congenital anomalies: a case report.

Authors:  Muna A Al Dhaibani; Diane Allingham-Hawkins; Ayman W El-Hattab
Journal:  BMC Med Genet       Date:  2017-10-23       Impact factor: 2.103

4.  Prenatal identification of two discontinuous maternally inherited chromosome 7q36.3 microduplications totaling 507 kb including the sonic hedgehog gene in a fetus with multiple congenital anomalies.

Authors:  Mark Micale; Bedford Embrey; Katie Hubbell; Kelly Beaudry-Rogers; Amy Whitten
Journal:  Clin Case Rep       Date:  2017-05-10
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.