2019
DOI: 10.3339/jkspn.2019.23.2.111
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Vitamin D Dependent Rickets Type 1A Caused by <i>CYP27B1</i> Mutation

Abstract: Vitamin D Dependent Rickets Type 1A Caused by CYP27B1 Mutation Vitamin D dependent rickets type 1A (VDDR1A) is an autosomal recessive disorder caused by mutations in CYP27B1. Clinical findings are growth retardation, hypotonia, muscle weakness, hypocalcemic seizures, and radiological features of rickets. We aimed to present the VDDR1A case with a genetic study of CYP27B1. The 14month-old boy was admitted to the hospital due to a seizure. Serum calcium, phosphorus, alkaline phosphatase, parathyroid hormone (PTH… Show more

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“…[1][2][3] Case reports of VDDR-1A, like in our patients, have been published recently, emphasizing that 1.25(OH)2D levels can be within normal ranges and this may explain difficulties in making the diagnosis. [11][12][13][14][15] On the other hand, VDDR-2 is characterized by resistance to 1.25 (OH) 2 D because of pathogenic variants in VDR (vitamin D receptor gene, VDDR-2A) or the overexpression of a nuclear ribonucleoprotein that interferes with vitamin D receptor-DNA interaction (VDDR-2B). 2,3 In these cases, 25(OH)D can be within normal or increased levels and 1.25(OH) 2 D is usually increased.…”
Section: Discussionmentioning
confidence: 99%
“…[1][2][3] Case reports of VDDR-1A, like in our patients, have been published recently, emphasizing that 1.25(OH)2D levels can be within normal ranges and this may explain difficulties in making the diagnosis. [11][12][13][14][15] On the other hand, VDDR-2 is characterized by resistance to 1.25 (OH) 2 D because of pathogenic variants in VDR (vitamin D receptor gene, VDDR-2A) or the overexpression of a nuclear ribonucleoprotein that interferes with vitamin D receptor-DNA interaction (VDDR-2B). 2,3 In these cases, 25(OH)D can be within normal or increased levels and 1.25(OH) 2 D is usually increased.…”
Section: Discussionmentioning
confidence: 99%