Novel large deletion involving EVC and EVC2 in Ellis-van Creveld syndrome
Hiroki Sato1, Kenichi Suga2, Masashi Suzue1
1Department of Pediatrics, Tokushima University Hospital, Kuramotocho, Tokushima, Japan.
Human Genome Variation
|May 17, 2022
Abstract:
Ellis-van Creveld syndrome is an autosomal recessive skeletal dysplasia that is characterized by thoracic hypoplasia, polydactyly, oral abnormalities, and congenital heart disease. It is caused by pathogenic variants in the EVC or EVC2 genes. We report a case of a newborn with a compound heterozygous variant comprising NM_147127.5: c.1991dup:[p.Lys665Glufs*10] in the EVC2 gene and a novel large deletion involving exon 1 in EVC and exons 1-7 in EVC2.
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