| Literature DB >> 32473227 |
Veronica Arora1, Eyby Leon2, Jullianne Diaz2, Hanne Buciek Hove3, Daniel Rocha Carvalho4, Kenji Kurosawa5, Naoto Nishimura5, Gen Nishimura6, Renu Saxena7, Carlos Ferreira8, Ratna Dua Puri7, Ishwar C Verma9.
Abstract
Primrose syndrome (OMIM 259050) is a rare disorder characterised by macrocephaly with developmental delay, a recognisable facial phenotype, altered glucose metabolism, and other features such as sensorineural hearing loss, short stature, and calcification of the ear cartilage. It is caused by heterozygous variants in ZBTB20, a member of the POK family of transcription repressors. Recently, this gene was shown to have a role in skeletal development through its action on chondrocyte differentiation by repression of SOX9. We describe five unrelated patients with Primrose syndrome and distinct skeletal features including multiple Wormian bones, platybasia, bitemporal bossing, bathrocephaly, slender bones, epiphyseal and spondylar dysplasia. The radiological abnormalities of the skull and the epiphyseal dysplasia were the most consistent findings. This novel constellation of skeletal features expands the phenotypic spectrum of the disorder.Entities:
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Year: 2020 PMID: 32473227 PMCID: PMC9445699 DOI: 10.1016/j.ejmg.2020.103967
Source DB: PubMed Journal: Eur J Med Genet ISSN: 1769-7212 Impact factor: 2.465