Alzaid Mohammed, Alshamrani Abdullah, Al Harbi Adel S, Alenzi Ayed, Mohamed Sarar
Prince Sultan Military Medical City, Riyadh, Kingdom of Saudi Arabia. E-mail.
Saudi Med J. 2019 Feb;40(2):195-198. doi: 10.15537/smj.2019.2.23908.
The methionyl-tRNA synthetase (MARS) mutation is a very rare cause of congenital pulmonary alveolar proteinosis.We report a 6-month-old boy born with symmetrical intrauterine growth retardation presented with unexplained persistent tachypnea and hypoxemia associated with severe failure to thrive, anemia, hypoalbuminemia and hepatomegaly. Detailed pulmonary investigations including computed tomography chest scan, bronchoscopy and bronchoalveolar lavage revealed pulmonary alveolar proteinosis. Whole exome sequencing identified a homozygous novel variant in the MARS gene, c.854T>C p.(Ile285Thr).
甲硫氨酰 - tRNA合成酶(MARS)突变是先天性肺泡蛋白沉积症非常罕见的病因。我们报告一名6个月大的男婴,出生时患有对称性宫内生长迟缓,出现原因不明的持续性呼吸急促和低氧血症,伴有严重的生长发育迟缓、贫血、低白蛋白血症和肝肿大。详细的肺部检查,包括胸部计算机断层扫描、支气管镜检查和支气管肺泡灌洗,显示为肺泡蛋白沉积症。全外显子测序在MARS基因中鉴定出一个纯合的新变异,即c.854T>C p.(Ile285Thr)。