A COL4A1 variant in a neonate with multiple intracranial hemorrhages and congenital cataracts

一名新生儿携带COL4A1变异基因,并伴有多发性颅内出血和先天性白内障。

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Abstract

A 2-day-old neonate presented with seizures, multiple intracranial hemorrhages, and bilateral congenital cataracts. Targeted next-generation sequencing of the collagen type IV alpha 1 chain (COL4A1) gene revealed a heterozygous de novo missense variant (NM_001845.6:c.2291G>A/p.Gly764Asp). This missense variant adds to the compendium of COL4A1 variants and is associated with a COL4A1-related disorder.

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