Ellis-van Creveld syndrome in a patient from Tanzania

Dekker, M.C.J.; Sadiq, A.M.; Jusabani, M.A.; Mdavire, V.J.; Baas, F.; Morton, D.H.; Hannel, B.J. (2019)

Article / Letter to editor

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 The baby presented with polydactyly, short limbs and atrioventricular septal defect, but was withdrawn from clinical follow up for the first year of life.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.

• Ellis-van Creveld syndrome
• EVC2 gene mutations
• hematological abnormalities

• All authors: Dekker, M.C.J.; Sadiq, A.M.; Jusabani, M.A.; Mdavire, V.J.; Baas, F.; Morton, D.H.; Hannel, B.J.
• Date: 2019-07-26
• Journal: American Journal of Medical Genetics Part A
• Volume: 179
• Issue: 10
• Pages: 2034 - 2038
• DOI: doi:10.1002/ajmg.a.61309