{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T10:54:43Z","timestamp":1791284083059,"version":"4.1.0"},"reference-count":15,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2019,7,16]],"date-time":"2019-07-16T00:00:00Z","timestamp":1563235200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2019,7,16]],"date-time":"2019-07-16T00:00:00Z","timestamp":1563235200000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Acad Dermatol Venereol"],"published-print":{"date-parts":[[2020,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>\n                      From a dermatologist's perspective, there are four major types of cutaneous porphyrias (\n                      <jats:styled-content style=\"fixed-case\">CP<\/jats:styled-content>\n                      s): porphyria cutanea tarda (\n                      <jats:styled-content style=\"fixed-case\">PCT<\/jats:styled-content>\n                      ), erythropoietic protoporphyria (\n                      <jats:styled-content style=\"fixed-case\">EPP<\/jats:styled-content>\n                      ), variegate porphyria (\n                      <jats:styled-content style=\"fixed-case\">VP<\/jats:styled-content>\n                      ) and hereditary coproporphyria (\n                      <jats:styled-content style=\"fixed-case\">HCP<\/jats:styled-content>\n                      ). Scarce data are available regarding the epidemiology of\n                      <jats:styled-content style=\"fixed-case\">CP<\/jats:styled-content>\n                      s.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Objectives<\/jats:title>\n                    <jats:p>\n                      To describe the epidemiology of\n                      <jats:styled-content style=\"fixed-case\">CP<\/jats:styled-content>\n                      s in Israel, including distribution, incidence and prevalence rates of major types.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      This retrospective study includes all patients who were diagnosed with\n                      <jats:styled-content style=\"fixed-case\">CP<\/jats:styled-content>\n                      s between the years 1988\u20132018. It is based on data from Israel's National Service for the Biochemical Diagnoses of Porphyrias, and Israeli patients\u2019 nationwide electronic medical charts. Incidence and prevalence rates were calculated.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Of 173 patients with\n                      <jats:styled-content style=\"fixed-case\">CP<\/jats:styled-content>\n                      s diagnosed during a 30\u2010year period, 65 (38%) had\n                      <jats:styled-content style=\"fixed-case\">VP<\/jats:styled-content>\n                      , 62 (36%) had\n                      <jats:styled-content style=\"fixed-case\">PCT<\/jats:styled-content>\n                      , 31 (18%) had\n                      <jats:styled-content style=\"fixed-case\">HCP<\/jats:styled-content>\n                      and 15 (9%) had\n                      <jats:styled-content style=\"fixed-case\">EPP<\/jats:styled-content>\n                      ; with incidence rates of 0.29, 0.30, 0.17, 0.07, and prevalence rates of 6.3, 4.8, 2.9, 1.6, respectively, per million population. Characteristics of patients with\n                      <jats:styled-content style=\"fixed-case\">PCT<\/jats:styled-content>\n                      differed from those with other\n                      <jats:styled-content style=\"fixed-case\">CP<\/jats:styled-content>\n                      s with regard to lack of family history, older mean age at diagnosis [51 vs. 36 (\n                      <jats:styled-content style=\"fixed-case\">VP<\/jats:styled-content>\n                      ), 35 (\n                      <jats:styled-content style=\"fixed-case\">HCP<\/jats:styled-content>\n                      ) and 25 (\n                      <jats:styled-content style=\"fixed-case\">EPP<\/jats:styled-content>\n                      ) years] and male predominance (81% vs. similar distribution). All patients with\n                      <jats:styled-content style=\"fixed-case\">PCT<\/jats:styled-content>\n                      were diagnosed at adulthood, while 20%, 19% and 15% of patients with\n                      <jats:styled-content style=\"fixed-case\">VP<\/jats:styled-content>\n                      ,\n                      <jats:styled-content style=\"fixed-case\">HCP<\/jats:styled-content>\n                      and\n                      <jats:styled-content style=\"fixed-case\">EPP<\/jats:styled-content>\n                      , respectively, were diagnosed during childhood or adolescence.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      Variegate porphyria and\n                      <jats:styled-content style=\"fixed-case\">PCT<\/jats:styled-content>\n                      were found to be the most prevalent in Israel; however,\n                      <jats:styled-content style=\"fixed-case\">CP<\/jats:styled-content>\n                      s might be underdiagnosed, thus dermatologists\u2019 awareness of these rare disorders is highly important.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/jdv.15769","type":"journal-article","created":{"date-parts":[[2019,7,2]],"date-time":"2019-07-02T03:20:02Z","timestamp":1562037602000},"page":"184-187","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":6,"title":["Epidemiology of cutaneous porphyria in Israel: a nationwide cohort study"],"prefix":"10.1111","volume":"34","author":[{"given":"Y.","family":"Edel","sequence":"first","affiliation":[{"name":"National Service for the Biochemical Diagnoses of Porphyrias Rabin Medical Center Beilinson Hospital Petach Tikva Israel"},{"name":"Rheumatology Unit Rabin Medical Center Beilinson Hospital Petach Tikva Israel"},{"name":"Sackler Faculty of Medicine Tel Aviv University Tel Aviv Israel"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"R.","family":"Mamet","sequence":"additional","affiliation":[{"name":"National Service for the Biochemical Diagnoses of Porphyrias Rabin Medical Center Beilinson Hospital Petach Tikva Israel"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-7126-2193","authenticated-orcid":false,"given":"I.","family":"Snast","sequence":"additional","affiliation":[{"name":"Sackler Faculty of Medicine Tel Aviv University Tel Aviv Israel"},{"name":"Photodermatosis Clinic Department of Dermatology Beilinson Hospital Petach Tikva Israel"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"R.","family":"Kaftory","sequence":"additional","affiliation":[{"name":"Sackler Faculty of Medicine Tel Aviv University Tel Aviv Israel"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S.","family":"Mazor","sequence":"additional","affiliation":[{"name":"Department of Community Dentistry School of Dental Medicine Hebrew University\u2010Hadassah Medical Center Jerusalem Israel"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"E.","family":"Hodak","sequence":"additional","affiliation":[{"name":"Sackler Faculty of Medicine Tel Aviv University Tel Aviv Israel"},{"name":"Photodermatosis Clinic Department of Dermatology Beilinson Hospital Petach Tikva Israel"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M.","family":"Lapidoth","sequence":"additional","affiliation":[{"name":"Sackler Faculty of Medicine Tel Aviv University Tel Aviv Israel"},{"name":"Photodermatosis Clinic Department of Dermatology Beilinson Hospital Petach Tikva 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