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Oculofaciocardiodental syndrome caused by a novel BCOR variant
Tomoyo Yamashita1,2, Junko Hotta1,2, Yukiko Jogu1
1Department of Medical Genetics, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Abstract:
Oculofaciocardiodental syndrome is caused by variants in the BCL6 corepressor (BCOR) gene. We identified a novel heterozygous frameshift variant, NM_001123385.2(BCOR):c.2326del, that arose de novo in a Japanese girl with characteristic facial features, congenital heart disease, bilateral syndactyly of toes 2 and 3, congenital cataracts, dental abnormalities, and mild intellectual disability. Reports of BCOR variants are rare, and further case accumulation is warranted.
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