| Literature DB >> 33166063 |
Pavalan Selvam1, Angita Jain1, Anvir Cheema1, Herjot Atwal1, Irman Forghani2, Paldeep S Atwal1.
Abstract
Casein kinase 2-related disorders have been linked to pathogenic variants in CSNK2A1 and CSNK2B. CSNK2B-related disease is predominantly associated with neurodevelopmental abnormalities affecting cognition; however, the extent of the phenotype associated with CSNK2B pathogenic variants is yet to be fully explored. Here, we describe a patient with features suggestive of Poirier-Bienvenu neurodevelopmental syndrome, harboring a novel CSNK2B pathogenic variant. We also report that the linear growth abnormalities could be a recurrent presentation in patients with this syndrome and suggest the effect of growth hormone therapy in our patient's stature.Entities:
Keywords: CSNK2B; dopamine; intellectual disability; seizures; stature
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Year: 2020 PMID: 33166063 DOI: 10.1002/ajmg.a.61960
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802