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A rare homozygous missense mutation of COL7A1 in a Vietnamese family.

Authors :
Duong, Nguyen Thuy
Anh, Luong Thi Lan
Sau, Nguyen Huu
Anh, Nguyen Bao
Miyake, Noriko
Van Hai, Nong
Matsumoto, Naomichi
Source :
Human Genome Variation; 6/6/2022, Vol. 9 Issue 1, p1-4, 4p
Publication Year :
2022

Abstract

We present a homozygous missense mutation in the COL7A1 gene (NM_000094.4: c.6262G>A, p.G2088R) in a case of inversa recessive dystrophic epidermolysis bullosa (RDEB-I) from a nonconsanguineous Vietnamese family. Although a heterozygous form of this mutation in combination with a premature termination codon allele has been shown to cause RDEB-I, this is the first report of homozygosity of this mutation as the etiology. Here, we investigated the molecular basis of the patient's disease for prenatal diagnosis after genetic counseling of the parents. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
2054345X
Volume :
9
Issue :
1
Database :
Complementary Index
Journal :
Human Genome Variation
Publication Type :
Academic Journal
Accession number :
157280266
Full Text :
https://doi.org/10.1038/s41439-022-00192-y