{"title":"Metabolic Bone Disease: An Overview.","authors":"Catherine Gooch, Paige Ekert, Gary S Gottesman","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Metabolic bone diseases are a heterogenous group of conditions that all result in aberrant bone mineral homeostasis with resulting skeletal disease. The underlying causes are variable, ranging from nutritional deficiencies to pathogenic variants in skeletal genes. To properly diagnose and treat these conditions, a clinician needs to understand bone metabolism as well as recognize the signs of disease in a patient. This review will focus on three relatively common metabolic bone diseases (osteogenesis imperfecta, hypophosphatasia, and X-linked hypophosphatemic rickets) that are caused by genetic variants, not by nutritional deficiency. As molecular DNA sequencing has improved, the scientific community has been able to better understand the genetic basis of these conditions and create sophisticated medical treatments based on the genetic deficiency.</p>","PeriodicalId":74203,"journal":{"name":"Missouri medicine","volume":"121 4","pages":"297-303"},"PeriodicalIF":0.0000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11578561/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Missouri medicine","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Metabolic bone diseases are a heterogenous group of conditions that all result in aberrant bone mineral homeostasis with resulting skeletal disease. The underlying causes are variable, ranging from nutritional deficiencies to pathogenic variants in skeletal genes. To properly diagnose and treat these conditions, a clinician needs to understand bone metabolism as well as recognize the signs of disease in a patient. This review will focus on three relatively common metabolic bone diseases (osteogenesis imperfecta, hypophosphatasia, and X-linked hypophosphatemic rickets) that are caused by genetic variants, not by nutritional deficiency. As molecular DNA sequencing has improved, the scientific community has been able to better understand the genetic basis of these conditions and create sophisticated medical treatments based on the genetic deficiency.
代谢性骨病是一组不同的疾病,它们都会导致骨矿物质平衡失调,从而引起骨骼疾病。其根本原因多种多样,从营养缺乏到骨骼基因中的致病变异,不一而足。为了正确诊断和治疗这些疾病,临床医生需要了解骨代谢,并识别患者的疾病征兆。本综述将重点讨论三种相对常见的代谢性骨病(成骨不全症、低磷血症和 X 连锁低磷血症佝偻病),它们是由基因变异而非营养缺乏引起的。随着分子 DNA 测序技术的进步,科学界能够更好地了解这些疾病的遗传基础,并根据遗传缺陷创造出先进的医疗方法。