{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Rosenhahn E"],"funding":["Medical Research Council"],"pagination":["1421-1435"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9388382"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["109(8)"],"pubmed_abstract":["PPFIBP1 encodes for the liprin-β1 protein, which has been shown to play a role in neuronal outgrowth and synapse formation in Drosophila melanogaster. By exome and genome sequencing, we detected nine ultra-rare homozygous loss-of-function variants in 16 individuals from 12 unrelated families. The individuals presented with moderate to profound developmental delay, often refractory early-onset epilepsy, and progressive microcephaly. Further common clinical findings included muscular hyper- and hypotonia, spasticity, failure to thrive and short stature, feeding difficulties, impaired vision, and congenital heart defects. Neuroimaging revealed abnormalities of brain morphology with leukoencephalopathy, ventriculomegaly, cortical abnormalities, and intracranial periventricular calcifications a"],"journal":["American journal of human genetics"],"pubmed_title":["Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications."],"pmcid":["PMC9388382"],"funding_grant_id":["MC_UP_1102/6","MC-A658-5TY30"],"pubmed_authors":["Tabarki B","Al Safar AH","Alhashem A","Hussien H","Gleeson JG","Brown AEX","Seyedhassani SM","Zaki MS","Rostasy K","Maroofian R","Correia SP","Alavi S","Wieczorek D","Bubshait DK","Platzer K","Rosenhahn E","Morsy H","Tajsharghi H","Hashem MO","Lemke JR","Omrani A","Houlden H","Zanobio M","Brunetti-Pierri N","Vitobello A","Alahmady NF","Harzallah I","Ghavideldarestani M","Omar TEI","Shahrooei M","Hentschel J","Sticht H","Abou Jamra R","Ebrahimi Nasab M","Torella A","Ygberg S","Nambot S","Alkuraya FS","Wredenberg A","O'Brien TJ","Lesko N","Terrone G","Alamri AS","Abdel-Salam GMH","Sorge I","Abdel-Hamid MS","Touraine R"],"additional_accession":[]},"is_claimable":false,"name":"Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications.","description":"PPFIBP1 encodes for the liprin-β1 protein, which has been shown to play a role in neuronal outgrowth and synapse formation in Drosophila melanogaster. By exome and genome sequencing, we detected nine ultra-rare homozygous loss-of-function variants in 16 individuals from 12 unrelated families. The individuals presented with moderate to profound developmental delay, often refractory early-onset epilepsy, and progressive microcephaly. Further common clinical findings included muscular hyper- and hypotonia, spasticity, failure to thrive and short stature, feeding difficulties, impaired vision, and congenital heart defects. Neuroimaging revealed abnormalities of brain morphology with leukoencephalopathy, ventriculomegaly, cortical abnormalities, and intracranial periventricular calcifications a","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Aug","modification":"2026-05-27T11:05:24.902Z","creation":"2025-02-19T00:13:27.741Z"},"accession":"S-EPMC9388382","cross_references":{"pubmed":["35830857"],"doi":["10.1016/j.ajhg.2022.06.008"]}}