| Literature DB >> 32895917 |
Maryam Beheshtian1, Tara Akhtarkhavari1, Sepideh Mehvari1, Marzieh Mohseni1, Zohreh Fattahi1, Seyedeh Sedigheh Abedini1, Sanaz Arzhangi1, Mahsa Fadaee1, Payman Jamali2, Reza Najafipour3, Vera M Kalscheuer4, Hao Hu5, Hans-Hilger Ropers4,6, Hossein Najmabadi1,7, Kimia Kahrizi1.
Abstract
Mutations in adaptor protein complex-4 (AP-4) genes have first been identified in 2009, causing a phenotype termed as AP-4 deficiency syndrome. Since then several patients with overlapping phenotypes, comprised of intellectual disability (ID) and spastic tetraplegia have been reported. To delineate the genotype-phenotype correlation of the AP-4 deficiency syndrome, we add the data from 30 affected individuals from 12 out of 640 Iranian families with ID in whom we detected disease-causing variants in AP-4 complex subunits, using next-generation sequencing. Furthermore, by comparing genotype-phenotype findings of those affected individuals with previously reported patients, we further refine the genotype-phenotype correlation in this syndrome. The most frequent reported clinical findings in the 101 cases consist of ID and/or global developmental delay (97%), speech disorders (92.1%), inability to walk (90.1%), spasticity (77.2%), and microcephaly (75.2%). Spastic tetraplegia has been reported in 72.3% of the investigated patients. The major brain imaging findings are abnormal corpus callosum morphology (63.4%) followed by ventriculomegaly (44.5%). Our result might suggest the AP-4 deficiency syndrome as a major differential diagnostic for unknown hereditary neurodegenerative disorders.Entities:
Keywords: AP-4 deficiency syndrome; Iranian families; consanguinity; genotype-phenotype correlation; intellectual disability
Year: 2020 PMID: 32895917 DOI: 10.1111/cge.13845
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438