{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,13]],"date-time":"2026-10-13T02:45:36Z","timestamp":1791859536308,"version":"4.3.4"},"reference-count":9,"publisher":"Wiley","issue":"9","license":[{"start":{"date-parts":[[2016,7,29]],"date-time":"2016-07-29T00:00:00Z","timestamp":1469750400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2016,7,29]],"date-time":"2016-07-29T00:00:00Z","timestamp":1469750400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"funder":[{"name":"Facult\u00e9 de Biologie et M\u00e9decine de l'Universit\u00e9 de Lausanne","id":[{"id":"https:\/\/ror.org\/019whta54","id-type":"ROR","asserted-by":"crossref"}]},{"name":"The SNF","award":["156260"],"award-info":[{"award-number":["156260"]}]},{"name":"The Leenaards Foundation, Lausanne"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Arthritis &amp; Rheumatology"],"published-print":{"date-parts":[[2016,9]]},"abstract":"<jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>To establish a diagnosis and provide counseling and treatment for 3 adult patients from one family presenting with peripheral osteolysis.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>Following clinical and radiographic assessment, exome sequencing, targeted gene resequencing, and determination of enzyme activity in cultured fibroblasts were performed.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      The proband (age 40 years) had a history of episodic fever and pain in childhood that subsided around puberty. He and 2 of his older sisters (ages 58 and 60 years, respectively) showed adult\u2010onset progressive shortening of fingers and toes with redundancy of the overlying skin. Radiographs showed severe osteolysis of the distal radius and ulna, carpal bones, metacarpal bones, and phalanges. Sequencing of the known genes for recessively inherited osteolysis,\n                      <jats:italic>MMP2<\/jats:italic>\n                      and\n                      <jats:italic>MMP14<\/jats:italic>\n                      , failed to show pathogenic mutations. Exome sequencing revealed compound heterozygosity for mutations c.505T&gt;C (p.Trp169Arg) and c.760A&gt;G (p.Arg254Gly) in\n                      <jats:italic>ASAH1<\/jats:italic>\n                      , the gene coding for acid ceramidase. Sanger sequencing confirmed correct segregation in the family, and enzyme activity in fibroblast cultures from the patients was reduced to \u223c8% of that in controls, confirming a diagnosis of Farber's disease.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      Our findings indicate that hypomorphic mutations in\n                      <jats:italic>ASAH1<\/jats:italic>\n                      may result in an osteoarticular phenotype with a juvenile phase resembling rheumatoid arthritis that evolves to osteolysis as the final stage in the absence of neurologic signs. This observation delineates a novel type of recessively inherited peripheral osteolysis and illustrates the long\u2010term skeletal manifestations of acid ceramidase deficiency (Farber's disease) in what appear to be the oldest affected individuals known so far.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1002\/art.39659","type":"journal-article","created":{"date-parts":[[2016,3,6]],"date-time":"2016-03-06T02:39:49Z","timestamp":1457231989000},"page":"2323-2327","source":"Crossref","is-referenced-by-count":21,"title":["Brief Report: Peripheral Osteolysis in Adults Linked to\n                    <i>ASAH1<\/i>\n                    (Acid Ceramidase) Mutations: A New Presentation of Farber's Disease"],"prefix":"10.1002","volume":"68","author":[{"given":"Luisa","family":"Bonaf\u00e9","sequence":"first","affiliation":[{"name":"Lausanne University Hospital and University of Lausanne Lausanne Switzerland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ariana","family":"Kariminejad","sequence":"additional","affiliation":[{"name":"Kariminejad\u2010Najmabadi Pathology and Genetics Centre Tehran Iran"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jia","family":"Li","sequence":"additional","affiliation":[{"name":"University of Lausanne Lausanne Switzerland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Beryl","family":"Royer\u2010Bertrand","sequence":"additional","affiliation":[{"name":"University of Lausanne Lausanne Switzerland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Virginie","family":"Garcia","sequence":"additional","affiliation":[{"name":"Centre Hospitalier Universitaire de Toulouse, INSERM UMR1037, and Universit\u00e9 Toulouse III Paul\u2010Sabatier Toulouse 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Hospitalier Universitaire de Toulouse, INSERM UMR1037, and Universit\u00e9 Toulouse III Paul\u2010Sabatier Toulouse France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Andrea","family":"Superti\u2010Furga","sequence":"additional","affiliation":[{"name":"Lausanne University Hospital and University of Lausanne Lausanne Switzerland"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2016,7,29]]},"reference":[{"key":"e_1_2_6_2_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.37365"},{"key":"e_1_2_6_3_1","doi-asserted-by":"publisher","DOI":"10.1038\/srep17154"},{"key":"e_1_2_6_4_1","doi-asserted-by":"publisher","DOI":"10.1194\/jlr.D010033"},{"key":"e_1_2_6_5_1","doi-asserted-by":"publisher","DOI":"10.1007\/s10545-012-9573-z"},{"key":"e_1_2_6_6_1","volume-title":"Online metabolic and molecular bases of inherited disease (OMMBID)","author":"Levade 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