Intracerebral hemorrhage is rare in term born neonates. Besides several non-genetic risk factors, pathogenic variants in COL4A1 and COL4A2 have been described to play a role in the pathophysiology of neonatal intracerebral hemorrhage. To the best of our knowledge, no intragenic COL4A2 duplications have been reported in humans to date. We report a neonate with intracerebral hemorrhage and a de novo intragenic COL4A2 duplication. Although it is not clear yet whether this genetic factor fully explains the clinical phenotype, it may have contributed at least as a risk factor for cerebral hemorrhage. Screening for intragenic COL4A1 and COL4A2 duplications as part of collagen IV diagnostics should be considered as part of the fetal and neonatal work-up for unexplained cerebral hemorrhages and to collect more evidence of the pathogenicity of this genetic mechanism.
CITATION STYLE
Koene, S., Peeters-Scholte, C. M. P. C. D., Knijnenburg, J., de Vries, L. S., van Scheltema, P. N. A., Meuwissen, M. E., … Santen, G. W. E. (2021). Intracerebral hemorrhage in a neonate with an intragenic COL4A2 duplication. American Journal of Medical Genetics, Part A, 185(2), 571–574. https://doi.org/10.1002/ajmg.a.61988
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