Acharya Sonu
Reader, Department of Pedodontics and Preventive Dentistry, Institute of Dental Sciences, Bhubaneswar, Odisha, India.
Int J Clin Pediatr Dent. 2015 May-Aug;8(2):141-4. doi: 10.5005/jp-journals-10005-1301. Epub 2015 Aug 11.
Sickle cell anemia is a genetic disease that primarily affects the black population. This anemia is due to a homozygous state of the abnormal hemoglobin S. An alteration occurs on the DNA molecule involving the substitution of the amino acid valine for glutamic acid at the sixth position on the beta polypeptide chain. This biochemical variation on the DNA molecule creates a physiological change that causes sickle-shaped red blood cells to be produced. The sickle-shaped cells are the result of the hemoglobin S being deoxygenated. This case report presents a case of 16-year-old female with sickle cell disease and its dental management. How to cite this article: Acharya S. Oral and Dental Considerations in Management of Sickle Cell Anemia. Int J Clin Pediatr Dent 2015;8(2):141-144.
镰状细胞贫血是一种主要影响黑人种群的遗传性疾病。这种贫血是由于异常血红蛋白S的纯合状态所致。DNA分子发生改变,涉及β多肽链第六位上的氨基酸缬氨酸取代谷氨酸。DNA分子上的这种生化变异产生了一种生理变化,导致生成镰状红细胞。镰状细胞是血红蛋白S脱氧的结果。本病例报告介绍了一名患有镰状细胞病的16岁女性病例及其牙科治疗情况。如何引用本文:阿查里亚S。镰状细胞贫血治疗中的口腔和牙科考量。《国际临床儿科牙科学杂志》2015年;8(2):141 - 144。