# Factor XIII Deficiency: A Silent Bleeder Behind a Normal Coagulation Profile

**Authors:** Ramesh Yadav, Madhav Raj Karki, Dikshya Pokhrel, Aron Neupane, Kshitiz Parajuli, Hem Sagar Rimal

PMC · DOI: 10.1002/ccr3.72193 · 2026-03-06

## TL;DR

A rare bleeding disorder, factor XIII deficiency, can go undetected in standard tests, leading to severe complications if not diagnosed and treated promptly.

## Contribution

This case highlights the diagnostic challenges of factor XIII deficiency and the need for targeted testing in resource-limited settings.

## Key findings

- Routine coagulation tests may appear normal despite factor XIII deficiency.
- Delayed diagnosis can lead to severe complications like epidural hematoma.
- Fresh frozen plasma and prophylactic care can effectively manage the condition.

## Abstract

Factor XIII deficiency is a rare cause of bleeding disorder. An 8‐month‐old male infant presented with persistent bleeding from a minor lip cut injury, which was sustained 2 days prior. The bleeding did not stop despite local hemostatic measures. His medical history was notable for spontaneous intradermal bleeds at different times and umbilical stump bleeding during the neonatal period. On examination, there were multiple petechiae and a large ecchymosis over the chest. Routine hematological and coagulation parameters were within normal limits. von Willebrand factor, factor VIII, and factor IX levels were normal. However, a qualitative 5M urea clot solubility test followed by factor XIII assay yielded abnormal results, confirming factor XIII deficiency. The patient was managed with fresh frozen plasma (FFP) and supportive care. Four months later, the patient presented with lethargy and vomiting, later diagnosed as epidural hematoma. The patient received FFP, had a favorable stay in the pediatric intensive care unit, and was discharged with no neurological deficits and a prophylactic plan. This case underscores how factor XIII deficiency can elude detection in routine coagulation tests, emphasizing the importance of prompt diagnosis and timely administration of replacement therapy to prevent complications and associated constraints in a resource limited setting.

Factor XIII deficiency can elude detection in routine coagulation tests in developing countries, emphasizing the importance of prompt diagnosis and timely administration of replacement therapy to prevent complications.

## Linked entities

- **Diseases:** Factor XIII deficiency (MONDO:0002241)

## Full-text entities

- **Genes:** F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}, F9 (coagulation factor IX) [NCBI Gene 2158] {aka F9 p22, FIX, HEMB, P19, PTC, THPH8}, F13A1 (coagulation factor XIII A chain) [NCBI Gene 2162] {aka F13A}, VWF (von Willebrand factor) [NCBI Gene 7450] {aka F8VWF, VWD}
- **Diseases:** coagulopathies (MESH:D001778), inherited bleeding disorder (MESH:D025861), lethargy (MESH:D053609), joint pain or swelling (MESH:D018771), organomegaly (MESH:D016878), death (MESH:D003643), skin discoloration (MESH:D014075), blood (MESH:D006402), Leukemia (MESH:D007938), intracranial bleeding (MESH:D013345), cerebral bleeding (MESH:D002543), disseminated intravascular coagulation (MESH:D004211), Congenital factor XIII deficiency (MESH:D005177), congenital factor deficiencies (MESH:D006467), hemophilia A or B (MESH:D002836), petechiae (MESH:D011693), bruising (MESH:D003288), Scalp swelling (MESH:D004476), inflammatory bowel disease (MESH:D015212), allergic reactions (MESH:D004342), battered baby syndrome (MESH:D001497), blood loss (MESH:D016063), ecchymoses (MESH:D004438), edema (MESH:D004487), liver disease (MESH:D008107), cut injury (MESH:D014947), hematoma (MESH:D006406), platelet function disorders (MESH:D001791), head trauma (MESH:D006259), fracture (MESH:D050723), clotting factor deficiency (MESH:C564885), neurological deficits (MESH:D009461), fever (MESH:D005334), systemic lupus erythematosus (MESH:D008180), vomiting (MESH:D014839), intracranial hemorrhage (MESH:D020300), rash (MESH:D005076), Bleeding (MESH:D006470), lip cut injury (MESH:D008047), nosebleeds (MESH:D004844), von Willebrand disease (MESH:D014842)
- **Chemicals:** urea (MESH:D014508), catridecacog (-), blood sugar (MESH:D001786)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12965841/full.md

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Source: https://tomesphere.com/paper/PMC12965841