J Genet Med.  2022 Dec;19(2):111-114. 10.5734/JGM.2022.19.2.111.

Variant of CHD1 gene resulting in a Korean case of Pilarowski-Bjornsson syndrome

• Sunwoo Y
• Seo SH
• Kim HJ
• Park MS
• Cho A

• KMID: 2537694
• DOI: http://doi.org/10.5734/JGM.2022.19.2.111

Abstract

Many monogenic neurodevelopmental disorders have been newly identified in recent years owing to the rapid development of genetic sequencing technology. These include variants of the epigenetic machinery – up to 300 known epigenetic factors of which about 50 have been linked to specific clinical phenotypes. Chromodomain, helicase, DNA binding 1 (CHD1) is an ATP-dependent chromatin remodeler, known to be the causative gene of the autosomal dominant neurodevelopmental disorder Pilarowski-Bjornsson syndrome. Patients exhibit various degrees of global developmental delay, autism, speech apraxia, seizures, growth retardation, and craniofacial dysmorphism. We report the first case of Pilarowski-Bjornsson syndrome in Korea, due to a de novo missense variant of the CHD1 gene (c.862A>G, p.Thr288Ala) in a previously undiagnosed 17-yearold male. His infantile onset of severe global developmental delay, intellectual disability, speech apraxia, and failure to thrive are compatible with Pilarowski-Bjornsson syndrome. We also noted some features not previously reported in this syndrome such as skeletal dysplasia and ichthyosis. Further studies are needed to discover the specific phenotypes and pathogenic mechanisms behind this rare disorder.

Keyword

Pilarowski-Bjornsson syndrome; CHD1; Neurodevelopmental disorder; Speech apraxia; Skeletal dysplasia