{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,31]],"date-time":"2025-10-31T19:35:27Z","timestamp":1761939327273,"version":"build-2065373602"},"reference-count":15,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2025,10,31]]},"DOI":"10.7759\/cureus.95841","type":"journal-article","created":{"date-parts":[[2025,10,31]],"date-time":"2025-10-31T19:29:49Z","timestamp":1761938989000},"source":"Crossref","is-referenced-by-count":0,"title":["Recurrent Intramuscular Hematoma Revealing Moderate Congenital Factor XIII Deficiency"],"prefix":"10.7759","author":[{"given":"Nada","family":"Ben Halima","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Salma","family":"Riahi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ines","family":"Mazlout","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Imen","family":"Mgarrech","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Amina","family":"Bouatay","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1097\/MOH.0b013e3283497e3e","article-title":"Novel aspects of factor XIII deficiency","volume":"18","author":"Muszbek L","year":"2011","unstructured":"Muszbek L, Bagoly Z, Cairo A, Peyvandi F. Novel aspects of factor XIII deficiency. Curr Opin Hematol. 2011, 18:366-72. 10.1097\/MOH.0b013e3283497e3e","journal-title":"Curr Opin Hematol"},{"key":"ref2","article-title":"Bleeding disorders due to congenital or acquired coagulation abnormalities: (excluding hemophilia and von Willebrand disease). (Article in French)","volume":"13021","author":"Denninger MH","year":"1985","unstructured":"Denninger MH, Huisse MG. Bleeding disorders due to congenital or acquired coagulation abnormalities: (excluding hemophilia and von Willebrand disease). (Article in French). Encycl Med Chir. 1985, 13021:C11.","journal-title":"Encycl Med Chir"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.1159\/000293395","article-title":"Congenital factor XIII deficiency with treatment of factor XIII concentrate and normal vaginal delivery","volume":"29","author":"Kobayashi T","year":"1990","unstructured":"Kobayashi T, Terao T, Kojima T, Takamatsu J, Kamiya T, Saito H. Congenital factor XIII deficiency with treatment of factor XIII concentrate and normal vaginal delivery. Gynecol Obstet Invest. 1990, 29:235-8. 10.1159\/000293395","journal-title":"Gynecol Obstet Invest"},{"key":"ref4","doi-asserted-by":"publisher","DOI":"10.2174\/187152508784871990","article-title":"The involvement of blood coagulation factor XIII in fibrinolysis and thrombosis","volume":"6","author":"Muszbek L","year":"2008","unstructured":"Muszbek L, Bagoly Z, Bereczky Z, Katona E. The involvement of blood coagulation factor XIII in fibrinolysis and thrombosis. Cardiovasc Hematol Agents Med Chem. 2008, 6:190-205. 10.2174\/187152508784871990","journal-title":"Cardiovasc Hematol Agents Med Chem"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.1111\/j.1538-7836.2012.04844.x","article-title":"Classification of rare bleeding disorders (RBDs) based on the association between coagulant factor activity and clinical bleeding severity","volume":"10","author":"Peyvandi F","year":"2012","unstructured":"Peyvandi F, Di Michele D, Bolton-Maggs PH, Lee CA, Tripodi A, Srivastava A. Classification of rare bleeding disorders (RBDs) based on the association between coagulant factor activity and clinical bleeding severity. J Thromb Haemost. 2012, 10:1938-43. 10.1111\/j.1538-7836.2012.04844.x","journal-title":"J Thromb Haemost"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.5482\/HAMO-13-08-0046","article-title":"Coagulation factor XIII deficiency. Diagnosis, prevalence and management of inherited\u00a0and\u00a0acquired forms","volume":"34","author":"Biswas A","year":"2014","unstructured":"Biswas A, Ivaskevicius V, Thomas A, Oldenburg J. Coagulation factor XIII deficiency. Diagnosis, prevalence and management of inherited\u00a0and\u00a0acquired forms. Hamostaseologie. 2014, 34:160-6. 10.5482\/HAMO-13-08-0046","journal-title":"Hamostaseologie"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.1111\/j.1538-7836.2011.04315.x","article-title":"Diagnosis and classification of factor XIII deficiencies","volume":"9","author":"Kohler HP","year":"2011","unstructured":"Kohler HP, Ichinose A, Seitz R, Ariens RA, Muszbek L. Diagnosis and classification of factor XIII deficiencies. J Thromb Haemost. 2011, 9:1404-6. 10.1111\/j.1538-7836.2011.04315.x","journal-title":"J Thromb Haemost"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.1684\/hma.2020.1571","article-title":"Congenital factor XIII deficiency in 2020: prevalence, clinical and biological diagnosis, and therapeutic modalities. (Article in French)","volume":"26","author":"Rugeri L","year":"2020","unstructured":"Rugeri L, Bouttefroy S, Jousselme E, Nougier C, Meunier S. Congenital factor XIII deficiency in 2020: prevalence, clinical and biological diagnosis, and therapeutic modalities. (Article in French). H\u00e9matologie. 2020, 26:192-200. 10.1684\/hma.2020.1571","journal-title":"H\u00e9matologie"},{"key":"ref9","doi-asserted-by":"publisher","DOI":"10.3109\/17453678508992981","article-title":"Bone healing stimulated by plasma factor XIII. Osteotomy experiments in sheep","volume":"56","author":"Claes L","year":"1985","unstructured":"Claes L, Burri C, Gerngross H, Mutschler W. Bone healing stimulated by plasma factor XIII. Osteotomy experiments in sheep. Acta Orthop Scand. 1985, 56:57-62. 10.3109\/17453678508992981","journal-title":"Acta Orthop Scand"},{"key":"ref10","doi-asserted-by":"publisher","DOI":"10.2450\/2014.0024-14","article-title":"Diagnosis and management of severe congenital factor XIII deficiency in the emergency department: lessons from a \"model\" family","volume":"13","author":"Bertamino M","year":"2015","unstructured":"Bertamino M, Banov L, Molinari AC. Diagnosis and management of severe congenital factor XIII deficiency in the emergency department: lessons from a \"model\" family. Blood Transfus. 2015, 13:324-7. 10.2450\/2014.0024-14","journal-title":"Blood Transfus"},{"key":"ref11","doi-asserted-by":"publisher","DOI":"10.1055\/s-0033-1353392","article-title":"Factor XIII deficiency: an update","volume":"39","author":"Schroeder V","year":"2013","unstructured":"Schroeder V, Kohler HP. Factor XIII deficiency: an update. Semin Thromb Hemost. 2013, 39:632-41. 10.1055\/s-0033-1353392","journal-title":"Semin Thromb Hemost"},{"key":"ref12","doi-asserted-by":"publisher","DOI":"10.1016\/j.patbio.2006.01.010","article-title":"Congenital factor XIII deficiency in the south of Tunisia. (Article in French)","volume":"54","author":"Medhaffar M","year":"2006","unstructured":"Medhaffar M, Elloumi M, Guermazi S, et al.. Congenital factor XIII deficiency in the south of Tunisia. (Article in French). Pathol Biol (Paris). 2006, 54:349-52. 10.1016\/j.patbio.2006.01.010","journal-title":"Pathol Biol (Paris)"},{"key":"ref13","doi-asserted-by":"publisher","DOI":"10.1016\/j.hoc.2021.07.009","article-title":"Factor XIII deficiency: a review of clinical presentation and management","volume":"35","author":"Pelcovits A","year":"2021","unstructured":"Pelcovits A, Schiffman F, Niroula R. Factor XIII deficiency: a review of clinical presentation and management. Hematol Oncol Clin North Am. 2021, 35:1171-80. 10.1016\/j.hoc.2021.07.009","journal-title":"Hematol Oncol Clin North Am"},{"key":"ref14","doi-asserted-by":"publisher","DOI":"10.1177\/10760296211024741","article-title":"Mild acquired factor XIII deficiency and clinical relevance at the ICU\u2014a retrospective analysis","volume":"27","author":"Schmitt FC","year":"2021","unstructured":"Schmitt FC, von der Forst M, Miesbach W, Casu S, Weigand MA, Alesci S. Mild acquired factor XIII deficiency and clinical relevance at the ICU\u2014a retrospective analysis. Clin Appl Thromb Hemost. 2021, 27:10.1177\/10760296211024741","journal-title":"Clin Appl Thromb Hemost"},{"key":"ref15","doi-asserted-by":"publisher","DOI":"10.1016\/j.annfar.2012.01.023","article-title":"Spontaneous intracerebral haemorrhage secondary to congenital factor XIII deficiency. (Article in French)","volume":"31","author":"El Koraichi A","year":"2012","unstructured":"El Koraichi A, Armel B, Nebhani T, Machkour Y, El Haddoury M, El Kettani SE. Spontaneous intracerebral haemorrhage secondary to congenital factor XIII deficiency. (Article in French). Ann Fr Anesth Reanim. 2012, 31:475-77. 10.1016\/j.annfar.2012.01.023","journal-title":"Ann Fr Anesth Reanim"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/419411-recurrent-intramuscular-hematoma-revealing-moderate-congenital-factor-xiii-deficiency","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,10,31]],"date-time":"2025-10-31T19:29:50Z","timestamp":1761938990000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/419411-recurrent-intramuscular-hematoma-revealing-moderate-congenital-factor-xiii-deficiency"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,10,31]]},"references-count":15,"URL":"https:\/\/doi.org\/10.7759\/cureus.95841","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2025,10,31]]}}}