Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 571-574 |
| Number of pages | 4 |
| Journal | American Journal of Medical Genetics. Part A |
| Volume | 185 |
| Issue number | 2 |
| Early online date | 28 Nov 2020 |
| DOIs | |
| Publication status | Published - Feb 2021 |
| Externally published | Yes |
Keywords
- COL4A2
- antenatal intracerebral hemorrhage
- neonatal intracerbral haemorrhage
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