Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, St Louis, Missouri, USA.
Child Abuse Pediatrics, Department of Pediatrics, Washington University School of Medicine, St Louis, Missouri, USA.
Am J Med Genet A. 2022 May;188(5):1538-1544. doi: 10.1002/ajmg.a.62647. Epub 2022 Jan 10.
Subdural hematoma (SDH) in infants raises the concern for nonaccidental trauma (NAT), especially when presenting with associated injuries. However, isolated SDH could be caused by multiple etiologies. NFIA (MIM# 600727) encodes nuclear factor I A protein (NFI-A), a transcription factor which plays important roles in gliogenesis. Loss-of-function variants in NFIA are associated with autosomal dominant brain malformations with or without urinary tract defects (MIM# 613735). Intracranial hemorrhage of various types besides SDH has been reported in patients with this condition. Here, we report a patient with a heterozygous novel NFIA pathogenic variant affecting splicing who initially presented with SDH concerning for NAT. We also review previous NFIA-related disorder cases with intracranial hemorrhage. This report emphasizes the importance of genetic evaluation in infants presenting with isolated SDH.
婴儿硬膜下血肿 (SDH) 引起人们对非故意伤害 (NAT) 的关注,尤其是当伴有其他损伤时。然而,孤立性 SDH 可能由多种病因引起。NFIA(MIM#600727)编码核因子 I A 蛋白 (NFI-A),一种转录因子,在神经发生中发挥重要作用。NFIA 的功能丧失变异与常染色体显性脑畸形有关,伴有或不伴有尿路缺陷 (MIM#613735)。除 SDH 外,该病症患者还报告有各种类型的颅内出血。在这里,我们报告了一名患者存在影响剪接的杂合性新型 NFIA 致病性变异,最初表现为 SDH 疑似 NAT。我们还回顾了以前 NFIA 相关疾病伴有颅内出血的病例。本报告强调了对出现孤立性 SDH 的婴儿进行基因评估的重要性。