Search Phenotypes

Ichthyosis, FA2H-related — Ichthyosis congenita (IC)

Jacinto et al. (2021): "Homozygosity mapping and whole-genome sequencing allowed the identification of a homozygous frameshift 1 bp insertion in the FA2H gene (c.9dupC; p.Ala4ArgfsTer142) located in a 1.92 Mb shared identical-by-descent region on chromosome 18 present in all cases, while the parents were heterozygous as expected for obligate carriers."

OMIA ID: 2450Inheritance: Jacinto et al. (2021): "pedigree records indicated a monogenic recessive trait."Characterised: YesYear: 2021