TY - JOUR
T1 - Defining the phenotypical spectrum associated with variants in TUBB2A
AU - Brock, Stefanie
AU - Vanderhasselt, Tim
AU - Vermaning, Sietske
AU - Keymolen, Kathelijn
AU - Régal, Luc
AU - Romaniello, Romina
AU - Wieczorek, Dagmar
AU - Storm, Tim Matthias
AU - Schaeferhoff, Karin
AU - Hehr, Ute
AU - Kuechler, Alma
AU - Krägeloh-Mann, Ingeborg
AU - Haack, Tobias B.
AU - Kasteleijn, Esmee
AU - Schot, Rachel
AU - Mancini, Grazia Maria Simonetta
AU - Webster, Richard
AU - Mohammad, Shekeeb
AU - Leventer, Richard J.
AU - Mirzaa, Ghayda
AU - Dobyns, William B.
AU - Bahi-Buisson, Nadia
AU - Meuwissen, Marije
AU - Jansen, Anna C.
AU - Stouffs, Katrien
N1 - Publisher Copyright:
©
PY - 2021/1/1
Y1 - 2021/1/1
N2 - Background Variants in genes belonging to the tubulin superfamily account for a heterogeneous spectrum of brain malformations referred to as tubulinopathies. Variants in TUBB2A have been reported in 10 patients with a broad spectrum of brain imaging features, ranging from a normal cortex to polymicrogyria, while one patient has been reported with progressive atrophy of the cerebellar vermis. Methods In order to further refine the phenotypical spectrum associated with TUBB2A, clinical and imaging features of 12 patients with pathogenic TUBB2A variants, recruited via the international network of the authors, were reviewed. Results We report 12 patients with eight novel and one recurrent variants spread throughout the TUBB2A gene but encoding for amino acids clustering at the protein surface. Eleven patients (91.7%) developed seizures in early life. All patients suffered from intellectual disability, and 11 patients had severe motor developmental delay, with 4 patients (36.4 %) being non-ambulatory. The cerebral cortex was normal in five individuals and showed dysgyria of variable severity in seven patients. Associated brain malformations were less frequent in TUBB2A patients compared with other tubulinopathies. None of the patients had progressive cerebellar atrophy. Conclusion The imaging phenotype associated with pathogenic variants in TUBB2A is highly variable, ranging from a normal cortex to extensive dysgyria with associated brain malformations. For recurrent variants, no clear genotype-phenotype correlations could be established, suggesting the role of additional modifiers.
AB - Background Variants in genes belonging to the tubulin superfamily account for a heterogeneous spectrum of brain malformations referred to as tubulinopathies. Variants in TUBB2A have been reported in 10 patients with a broad spectrum of brain imaging features, ranging from a normal cortex to polymicrogyria, while one patient has been reported with progressive atrophy of the cerebellar vermis. Methods In order to further refine the phenotypical spectrum associated with TUBB2A, clinical and imaging features of 12 patients with pathogenic TUBB2A variants, recruited via the international network of the authors, were reviewed. Results We report 12 patients with eight novel and one recurrent variants spread throughout the TUBB2A gene but encoding for amino acids clustering at the protein surface. Eleven patients (91.7%) developed seizures in early life. All patients suffered from intellectual disability, and 11 patients had severe motor developmental delay, with 4 patients (36.4 %) being non-ambulatory. The cerebral cortex was normal in five individuals and showed dysgyria of variable severity in seven patients. Associated brain malformations were less frequent in TUBB2A patients compared with other tubulinopathies. None of the patients had progressive cerebellar atrophy. Conclusion The imaging phenotype associated with pathogenic variants in TUBB2A is highly variable, ranging from a normal cortex to extensive dysgyria with associated brain malformations. For recurrent variants, no clear genotype-phenotype correlations could be established, suggesting the role of additional modifiers.
KW - clinical genetics
KW - epilepsy and seizures
KW - genetics
KW - neurology
KW - neurosciences
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U2 - 10.1136/jmedgenet-2019-106740
DO - 10.1136/jmedgenet-2019-106740
M3 - Article
C2 - 32571897
AN - SCOPUS:85091178288
SN - 0022-2593
VL - 58
SP - 33
EP - 40
JO - Journal of medical genetics
JF - Journal of medical genetics
IS - 1
ER -