Case report: Structural brain abnormalities in TUBA1A-tubulinopathies: a narrative review
- PMID: 37744437
- PMCID: PMC10515619
- DOI: 10.3389/fped.2023.1210272
Case report: Structural brain abnormalities in TUBA1A-tubulinopathies: a narrative review
Abstract
Introduction: Tubulin genes have been related to severe neurological complications and the term "tubulinopathy" now refers to a heterogeneous group of disorders involving an extensive family of tubulin genes with TUBA1A being the most common. A review was carried out on the complex and severe brain abnormalities associated with this genetic anomaly.
Methods: A literature review of the cases of TUBA1A-tubulopathy was performed to investigate the molecular findings linked with cerebral anomalies and to describe the clinical and neuroradiological features related to this genetic disorder.
Results: Clinical manifestations of TUBA1A-tubulinopathy patients are heterogeneous and severe ranging from craniofacial dysmorphism, notable developmental delay, and intellectual delay to early-onset seizures, neuroradiologically associated with complex abnormalities. TUBA1A-tubulinopathy may display various and complex cortical and subcortical malformations.
Discussion: A range of clinical manifestations related to different cerebral structures involved may be observed in patients with TUBA1A-tubulinopathy. Genotype-phenotype correlations are discussed here. Individuals with cortical and subcortical anomalies should be screened also for pathogenic variants in TUBA1A.
Keywords: DWM phenotype; Dandy–Walker Malformation; TUBA1A-tubulinopathy; cerebral anomalies; tubulinopathies.
© 2023 Pavone, Striano, Cacciaguerra, Marino, Parano, Pappalardo, Falsaperla and Ruggieri.
Conflict of interest statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Similar articles
-
Cross-sectional quantitative analysis of the natural history of TUBA1A and TUBB2B tubulinopathies.Genet Med. 2021 Mar;23(3):516-523. doi: 10.1038/s41436-020-01001-z. Epub 2020 Oct 21. Genet Med. 2021. PMID: 33082561 Free PMC article.
-
The mutational and phenotypic spectrum of TUBA1A-associated tubulinopathy.Orphanet J Rare Dis. 2019 Feb 11;14(1):38. doi: 10.1186/s13023-019-1020-x. Orphanet J Rare Dis. 2019. PMID: 30744660 Free PMC article. Review.
-
Complementing the phenotypical spectrum of TUBA1A tubulinopathy and its role in early-onset epilepsies.Eur J Hum Genet. 2022 Mar;30(3):298-306. doi: 10.1038/s41431-021-01027-0. Epub 2022 Jan 11. Eur J Hum Genet. 2022. PMID: 35017693 Free PMC article.
-
Broadening the phenotypic spectrum of TUBA1A tubulinopathy to syndromic arthrogryposis multiplex congenita.Am J Med Genet A. 2022 Aug;188(8):2331-2338. doi: 10.1002/ajmg.a.62866. Epub 2022 Jun 10. Am J Med Genet A. 2022. PMID: 35686685
-
Epilepsy in Tubulinopathy: Personal Series and Literature Review.Cells. 2019 Jul 2;8(7):669. doi: 10.3390/cells8070669. Cells. 2019. PMID: 31269740 Free PMC article. Review.
Cited by
-
Concurrent Dandy-Walker malformation and persistent fetal vasculature: A case report.Int J Surg Case Rep. 2024 Oct;123:110270. doi: 10.1016/j.ijscr.2024.110270. Epub 2024 Sep 10. Int J Surg Case Rep. 2024. PMID: 39307028 Free PMC article.
-
Lissencephaly caused by a de novo mutation in tubulin TUBA1A: a case report and literature review.Front Pediatr. 2024 May 14;12:1367305. doi: 10.3389/fped.2024.1367305. eCollection 2024. Front Pediatr. 2024. PMID: 38813542 Free PMC article.
References
Publication types
LinkOut - more resources
Full Text Sources