A case of pachydermoperiostosis caused by a deletion mutation in the HPGD gene

VernacularTitle:HPGD基因缺失突变致厚皮性骨膜病一例
Author: Chenzhao DING ; Lei REN ; Hao YUE ; Jing LI ; Tianxue ZHAO ; Guijun QIN
Publication Type:Journal Article
Keywords: Osteoarthropathy,primary hypertrophic; Mutation; HPGD gene; SLCO2A1 gene
From: Chinese Journal of Dermatology 2016;49(1):47-49
CountryChina
Language:Chinese
Abstract: Objective To confirm a case of pachydermoperiostosis (primary hypertrophic osteoarthropathy) at the molecular level by gene sequencing.Methods Peripheral blood samples were obtained from a 26-year-old male patient with pachydermoperiostosis and his parents,and DNA was extracted from these blood samples.Polymerase chain reaction (PCR) was performed to amplify all the exons of HPGD and SLCO2A1 genes,and gene sequencing to identify gene mutations.According to sequencing results,the spatial structure of relevant proteins was predicted.Results Gene sequencing showed a homozygous frame-shifting mutation c.310_31 1delCT (p.L104AfsX3) in exon 3 of the HPGD gene in the patient.His mother was a heterozygous carrier of the mutation,but no mutation was identified in his father.The prediction of spacial structure of proteins revealed that the above gene mutation could shorten the length of the encoded peptide by about 60％.Conclusion Typical clinical manifestations and imaging findings are helpful for the primary diagnosis of pachydermoperiostosis,while mutation analysis of HPGD and SLCO2A1 genes is a main approach to its final diagnosis.