<?xml version="1.0" encoding="UTF-8"?> <!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.2d1 20170631//EN" "JATS-journalpublishing1.dtd"> <ArticleSet> <Article> <Journal> <PublisherName>jimrhs</PublisherName> <JournalTitle>Journal of International Medical Research and Health Sciences</JournalTitle> <PISSN>I</PISSN> <EISSN>S</EISSN> <Volume-Issue>Volume 1 Issue 1</Volume-Issue> <PartNumber/> <IssueTopic>Multidisciplinary</IssueTopic> <IssueLanguage>English</IssueLanguage> <Season>(Apr-Jun, 2021)</Season> <SpecialIssue>N</SpecialIssue> <SupplementaryIssue>N</SupplementaryIssue> <IssueOA>Y</IssueOA> <PubDate> <Year>2021</Year> <Month>06</Month> <Day>4</Day> </PubDate> <ArticleType>Neurology</ArticleType> <ArticleTitle>Sporadic Fahr’s disease in Valle Camonica: Two case reports</ArticleTitle> <SubTitle/> <ArticleLanguage>English</ArticleLanguage> <ArticleOA>Y</ArticleOA> <FirstPage>23</FirstPage> <LastPage>28</LastPage> <AuthorList> <Author> <FirstName>Maria Sofia</FirstName> <LastName>Cotelli</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>N</CorrespondingAuthor> <ORCID/> <FirstName>Filippo</FirstName> <LastName>Manelli</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>Y</CorrespondingAuthor> <ORCID/> <FirstName>Stefano</FirstName> <LastName>Bonetti</LastName> <AuthorLanguage>English</AuthorLanguage> <Affiliation/> <CorrespondingAuthor>Y</CorrespondingAuthor> <ORCID/> </Author> </AuthorList> <DOI>2021.1104</DOI> <Abstract>Fahr__ampersandsign#39;s syndrome, or idiopathic basal ganglia calcification (IBGC), is a rare neurological disorder characterized by abnormal deposition of calcium in brain. The main clinical manifestations are rigid or hyperkinetic syndrome, mood disorders and cognitive impairment. It is usually inherited (known as familial idiopathic basal ganglia calcification) most commonly as an autosomal dominant trait, but it may also occur sporadically. We report two cases of sporadic Fahr’s disease in patients suffering from autoimmune, hematologic and metabolic disorders</Abstract> <AbstractLanguage>English</AbstractLanguage> <Keywords>Basal Ganglia, Calcifications, Autoimmune Diseases, Neurological Disorder</Keywords> <URLs> <Abstract>https://jimrhs.com/ubijournal-v1copy/journals/abstract.php?article_id=13070&title=Sporadic Fahr’s disease in Valle Camonica: Two case reports</Abstract> </URLs> <References> <ReferencesarticleTitle>References</ReferencesarticleTitle> <ReferencesfirstPage>16</ReferencesfirstPage> <ReferenceslastPage>19</ReferenceslastPage> <References>[1] Donzuso G, Mostile G, Nicoletti A, Zappia M, Basal ganglia calcifications (Fahrand;#39;s syndrome): related conditions and clinical features. Neurol Sci. 2019 Nov; 40(11):2251-2263. [2] Savino E, Soavi C, Capatti E, Borrelli M, Vigna GB, Passaro A, Zuliani G. Bilateral strio-pallido-dentate calcinosis (Fahr’s disease): report of seven cases and revision of literature. BMC Neurol. 2016; 16(1): 165. [3] Pistacchi M, Gioulis M, Sanson F, Marsala SM. Fahrand;#39;s syndrome and clinical correlation: a case series and literature review. Folia Neuropathol. 2016; 54(3):282-294. [4] Saleem S, Aslam HM, Anwar M, Anwar S, Saleem M, Saleem A, Rehmani MA. Fahrand;#39;s syndrome: literature review of current evidence. Orphanet J Rare Dis. 2013 Oct 8; 8:156. [5] Sobrid SH MJ, Geschwind DH. Familial Idiopathic Basal Ganglia Calcification: GeneReviews™ [Internet] Seattle (WA): University of Washington, Seattle; 2004. Updated 2007 Sep 20. [6] Horino T, Matsumoto T, Inoue K, Ichii O, Terada Y. Bilateral striopallidodentate calcinosis associated with Sjand;ouml;grenand;#39;s syndrome and IgDand;lambda; monoclonal gammopathy of undetermined significance. Joint Bone Spine. 2018 Mar; 85(2):243-245. doi: 10.1016/j.jbspin.2017.11.007. [7] Malik N, Pattan V, Nai Q, Hypoparathyroidism, Hypothyroidism and Thrombocytopenia: Rare Constellation of Fahr’s Syndrome. J Endocrinol Metab 2014 Aug 4; (4): 110-111 doi: 10.1176/appi.neuropsych.13100243. [8] Randhawa J, Onyshchenko M, Mbuvah F, Bagai R A Rare Association of Fahrand;#39;s Disease with an Autoimmune Triad. doi: 10.1176/appi.neuropsych.13100243.</References> </References> </Journal> </Article> </ArticleSet>