Choudhury Sangita, Jebasingh K Felix, Ranabir Salam, Singh Th Premchand
Department of Medicine, Regional InstitutWe of Medical Sciences, Imphal, Manipur, India.
Indian J Endocrinol Metab. 2013 Oct;17(Suppl 1):S224-7. doi: 10.4103/2230-8210.119579.
Rickets is softening of bones due to defective mineralization of cartilage in the epiphyseal growth plate, leading to widening of ends of long bones, growth retardation, and skeletal deformities in children. The predominant cause is deficiency or impaired metabolism of vitamin D. The observation that some forms of rickets could not be cured by regular doses of vitamin D, led to the discovery of rare inherited abnormalities of vitamin D metabolism or vitamin D receptor. Vitamin D dependent rickets (VDDR) is of two types: Type I is due to defective renal tubular 25-hydroxyvitamin D 1-α hydroxylase and type II is due to end-organ resistance to active metabolite of vitamin D. Typical signs are observed from the first month of life. The patient with rickets described below had markedly increased serum alkaline phosphatase and 1,25-dihydroxyvitamin D. We attribute these abnormalities to impaired end-organ responsiveness to 1,25-dihydroxyvitamin D.
佝偻病是由于骨骺生长板软骨矿化缺陷导致的骨骼软化,可致使儿童长骨末端增宽、生长发育迟缓以及骨骼畸形。主要病因是维生素D缺乏或代谢受损。一些类型的佝偻病无法通过常规剂量的维生素D治愈,这一观察结果促使人们发现了罕见的维生素D代谢或维生素D受体遗传性异常。维生素D依赖性佝偻病(VDDR)有两种类型:I型是由于肾小管25-羟维生素D 1-α羟化酶缺陷,II型是由于终末器官对维生素D活性代谢产物耐药。典型症状在出生后第一个月即可观察到。以下所述的佝偻病患者血清碱性磷酸酶和1,25-二羟维生素D显著升高。我们将这些异常归因于终末器官对1,25-二羟维生素D的反应性受损。