{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,12]],"date-time":"2026-10-12T05:45:50Z","timestamp":1791783950855,"version":"4.3.4"},"reference-count":23,"publisher":"Wiley","issue":"10","license":[{"start":{"date-parts":[[2026,10,11]],"date-time":"2026-10-11T00:00:00Z","timestamp":1791676800000},"content-version":"vor","delay-in-days":10,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,10,1]],"date-time":"2026-10-01T00:00:00Z","timestamp":1790812800000},"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":["Clinical Case Reports"],"published-print":{"date-parts":[[2026,10]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>In regions with high consanguinity, rare recessive disorders like Ullrich congenital muscular dystrophy (UCMD) may present at birth with hypotonia and respiratory distress. To enhance quality of life and prevent recurrence in future pregnancies, early recognition, genetic counseling, and care from a multidisciplinary team of specialists are essential.<\/jats:p>","DOI":"10.1002\/ccr3.73658","type":"journal-article","created":{"date-parts":[[2026,10,12]],"date-time":"2026-10-12T05:08:57Z","timestamp":1791781737000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Prevalence of Rare Diseases in Consanguineous Marriages: A Case of Ullrich Muscular Dystrophy in a Resource\u2010Limited Setting"],"prefix":"10.1002","volume":"14","author":[{"ORCID":"https:\/\/orcid.org\/0009-0002-6211-7522","authenticated-orcid":false,"given":"Kanza","family":"Farhan","sequence":"first","affiliation":[{"name":"Sindh Medical College Jinnah Sindh Medical University  Karachi Pakistan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0000-6908-0836","authenticated-orcid":false,"given":"Muhammad","family":"Burhan Tariq","sequence":"additional","affiliation":[{"name":"Sindh Medical College Jinnah Sindh Medical University  Karachi Pakistan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0007-7013-728X","authenticated-orcid":false,"given":"Amna","family":"Farhan","sequence":"additional","affiliation":[{"name":"Shaheed Mohtarma Benazir Bhutto Medical College, Lyari  Karachi Pakistan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0004-5457-1420","authenticated-orcid":false,"given":"Erma","family":"Khalid","sequence":"additional","affiliation":[{"name":"National Institute of Child Health\/National Institute of Cardiovascular Diseases  Karachi Pakistan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0001-1311-6403","authenticated-orcid":false,"given":"Suhaira","family":"Hafeez Syed","sequence":"additional","affiliation":[{"name":"Jinnah Postgraduate Medical Center  Karachi Pakistan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-1366-2375","authenticated-orcid":false,"given":"Mohammed Hammad Jaber","family":"Amin","sequence":"additional","affiliation":[{"name":"Faculty of Medicine Alzaiem Alazhari University  Khartoum Sudan"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2026,10,11]]},"reference":[{"issue":"1","key":"e_1_2_12_2_1","doi-asserted-by":"crossref","first-page":"338","DOI":"10.12998\/wjcc.v10.i1.338","article-title":"Clinical Manifestations and Prenatal Diagnosis of Ullrich Congenital Muscular Dystrophy: A Case Report","volume":"10","author":"Hu J.","year":"2022","journal-title":"World Journal of Clinical Cases"},{"key":"e_1_2_12_3_1","volume-title":"Muscular Dystrophies","author":"Griggs R. 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