Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2023 Sep 8:11:1210272.
doi: 10.3389/fped.2023.1210272. eCollection 2023.

Case report: Structural brain abnormalities in TUBA1A-tubulinopathies: a narrative review

Affiliations
Case Reports

Case report: Structural brain abnormalities in TUBA1A-tubulinopathies: a narrative review

Piero Pavone et al. Front Pediatr. .

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.

PubMed Disclaimer

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

Cited by

References

    1. Keays DA, Tian G, Poirier K, Huang GJ, Siebold C, Cleak J, et al. Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans. Cell. (2007) 128(1):45–57. 10.1016/j.cell.2006.12.017 - DOI - PMC - PubMed
    1. Di Donato N, Timms AE, Aldinger KA, Mirzaa GM, Bennett JT, Collins S, et al. Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephaly. Genet Med. (2018) 20(11):1354–64. 10.1038/gim.2018.8 - DOI - PMC - PubMed
    1. Tischfield MA, Cederquist GY, Gupta ML, Jr., Engle EC. Phenotypic spectrum of the tubulin- related disorders and functional implications of disease-causing mutations. Curr Opin Genet Dev. (2011) 21(3):286–94. 10.1016/j.gde.2011.01.003 - DOI - PMC - PubMed
    1. Bahi-Buisson N, Poirier K, Boddaert N, Saillour Y, Castelnau L, Philip N, et al. Refinement of cortical dysgeneses spectrum associated with TUBA1A mutations. J Med Genet. (2008) 45(10):647–53. 10.1136/jmg.2008.058073 - DOI - PubMed
    1. Hebebrand M, Hüffmeier U, Rollmann R, Keymolen K, Régal L, Romaniello R, et al. The mutational and phenotypic spectrum of TUBA1A-associated tubulinopathy. Orphanet J Rare Dis. (2019) 14(1):38. 10.1186/s13023-019-1020-x - DOI - PMC - PubMed

Publication types

LinkOut - more resources