Literature DB >> 23614707

Craniofrontonasal syndrome in a male due to chromosomal mosaicism involving EFNB1: further insights into a genetic paradox.

C Evers1, M S Jungwirth, J Morgenthaler, K Hinderhofer, B Maas, J W G Janssen, A Jauch, U Hehr, H Steinbeisser, U Moog.   

Abstract

Craniofrontonasal syndrome (CFNS) is an X-linked disorder caused by inactivating mutations in the gene for ephrin-B1 (EFNB1). Paradoxically it shows a more severe phenotype in females than in males. As a result of X inactivation cell populations with and without EFNB1 expression are found in EFNB1+/- females. This is thought to initiate a process termed cellular interference which may be responsible for the phenotype in females. We present a boy with severe clinical features of CFNS. In ∼42% of his blood cells we found a supernumerary ring X chromosome containing EFNB1 but lacking XIST. Mosaicism for cell populations with different levels of EFNB1 expression can explain the severe phenotype of this patient. In vitro experiments in Xenopus tissue showed that cells overexpress ephrinB1 cluster and sort out from wild-type cells. Our report provides further evidence that cellular interference contributes to the paradoxical inheritance pattern of CFNS.
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  EFNB1; craniofrontonasal syndrome; ephrin-B1; mosaicism; supernumerary ring X chromosome

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Year:  2013        PMID: 23614707     DOI: 10.1111/cge.12171

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  3 in total

1.  Genotype-phenotype correlation in 75 patients with small supernumerary marker chromosomes.

Authors:  Tingting Li; Haiquan Sang; Guoming Chu; Yuanyuan Zhang; Manlong Qi; Xiaoliang Liu; Wanting Cui; Yanyan Zhao
Journal:  Mol Cytogenet       Date:  2020-07-14       Impact factor: 2.009

2.  Isolated Sagittal Synostosis in a Boy with Craniofrontonasal Dysplasia and a Novel EFNB1 Mutation.

Authors:  Bharesh K Chauhan; Jacqueline M Hoover; Hannah Scanga; Anagha Medsinge; Georgianne L Arnold; Ken K Nischal
Journal:  Plast Reconstr Surg Glob Open       Date:  2015-07-08

3.  X-linked heterozygous mutations in ARR3 cause female-limited early onset high myopia.

Authors:  Xueshan Xiao; Shiqiang Li; Xiaoyun Jia; Xiangming Guo; Qingjiong Zhang
Journal:  Mol Vis       Date:  2016-10-26       Impact factor: 2.367

  3 in total

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