Hypoparathyroidism with situs inversus totalis:A case report  

作　　者：Mao Yang Sheng-Lan Pu Ling Li Yu Ma Qin Qin Yan-Xia Wang Wen-Long Huang Hong-Ya Hu Mei-Feng Zhu Chun-Zhu Li 

机构地区：[1]Department of General Medicine,First People’s Hospital of Zunyi(Third Affiliated Hospital of Zunyi Medical University),Zunyi 563000,Guizhou Province,China [2]Department of Nutrition,First People’s Hospital of Zunyi(Third Affiliated Hospital of Zunyi Medical University),Zunyi 563000,Guizhou Province,China

出　　处：《World Journal of Radiology》2024年第10期561-568,共8页世界放射学杂志（英文）

基　　金：Supported by Zunyi Science and Technology Plan Program No.HZ(2022)48;Zunyi Science and Technology Plan Program,No.HZ(2023)60.

摘　　要：BACKGROUND Hypoparathyroidism(HP)is a rare endocrine disorder,while situs inversus totalis(SIT)is a rare condition in which the internal organs are positioned in a mirrored pattern compared to their usual positions.This case illustrates some potential shared mechanisms between HP and SIT,highlighting the importance of accurate identification and prompt first emergency,offering insights for future research.CASE SUMMARY This report discusses a case of a middle-aged patient with adolescent-onset HP with concurrent SIT.The patient experienced recurrent episodes of increased neuromuscular excitability(manifesting as spasms in the hands and feet and laryngospasms)and even periods of unconsciousness.Initially,these symptoms led to a misdiagnosis of epilepsy.Nevertheless,upon thorough examination and treatment in the general medicine ward,the correct diagnosis was established.Corresponding treatment resulted in improved management of the patient’s symptoms.CONCLUSION Co-occurrence of HP and SIT may be associated with genetic mutations,chromosomal anomalies,or hereditary factors,as may other similar conditions.

关 键 词：HYPOPARATHYROIDISM Situs inversus totalis Consciousness disorder EPILEPSY Genetic inheritance Case report 

分 类 号：R697.3[医药卫生—泌尿科学]