Literature DB >> 31350806

Ellis-van Creveld syndrome in a patient from Tanzania.

Marieke C J Dekker1, Adnan M Sadiq2, Mubashir A Jusabani3, Vivian J Mdavire1, Frank Baas4, David H Morton5, Ben C J Hamel6.   

Abstract

We report an African infant with Ellis-van Creveld (EVC) syndrome. EVC syndrome is a chondral and ectodermal dysplasia with autosomal recessive transmission. The baby presented with polydactyly, short limbs and atrioventricular septal defect, but was withdrawn from clinical follow up for the first year of life. Initial hematological abnormalities could not be explained and normalized later. EVC syndrome was confirmed by genetic analysis that showed two pathogenic mutations in the EVC2 gene, c.653_654del, p.Val218Glyfs*12 in exon 5, and c.2710C>T, p.Gln904* in exon 16. The variant c.653_654del; p.Val218Glyfs*12 in exon 5 has not been described before. Our review of medical literature suggested this is the first molecularly confirmed case of EVC syndrome in sub-Saharan Africa.
© 2019 Wiley Periodicals, Inc.

Entities:  

Keywords:  zzm321990EVC2 gene mutations; Ellis-van Creveld syndrome; hematological abnormalities

Year:  2019        PMID: 31350806     DOI: 10.1002/ajmg.a.61309

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


  1 in total

1.  Microdeletion of 4p16.2 in Children: A Case Report and Literature Review.

Authors:  Yanjie Qian; Xiaoying Wang; Wei Tang; Chaochun Zou
Journal:  Case Rep Genet       Date:  2022-04-09
  1 in total

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