CONGENITAL FACTOR XIII DEFICIENCY
Altaf Naseem, U N Reddy
Department of Pediatrics, Deccan college of Medical Sciences, Hyderabad
Address for Correspondence
Dr. Altaf Naseem, Department of Pediatrics, Assistant Professor, Princess Esra Hospital, Shah ali Banda, Hyderabad - 500 002, Andhra Pradesh
Email
docaltaf@rediffmail.com
Keywords
Congenital Factor XIII deficiency, Bleeding diathesis, Cryoprecipitate
An eleven year old male child born of consanguineous marriage presented with pain in right lower abdomen and limping of right leg following trauma. On enquiring there was history of umbilical bleeding at birth, prolonged bleeding from cut injury, easy bruisability after trauma. He had received blood transfusion six times for bleeding in the past without any investigation. There was no history of similar complaints in other family members. On examination his general condition and vitals were stable, pallor was present. Ecchymosis over back, gluteal region and thighs was noticed. Movements at hip joint on right side were painful and restricted. All other systems were clinically normal. Complete blood count showed anemia. Coagulation screening tests were normal. Fibrinogen level was normal. Ultrasound abdomen showed right illiopsoas hematoma. Factor VIII and Factor IX levels were normal. Urea clot lyses showed abnormal solubility of clot in 5M urea. Factor XIII deficiency was thus confirmed. The child was given Fresh Frozen Plasma (FFP) and packed cell transfusion to treat anemia, and immunized with Hepatitis-B vaccine. He was advised to avoid NSAIDS, injuries and intramuscular injections. Child is doing well and receiving FFP every four weeks.

Congenital factor XIII deficiency, originally recognized by Duckert in 1960, is a rare autosomal recessive disease usually associated with a severe bleeding diathesis .(1) The incidence of this disease is about 1 case per 2-5 million population. The male to female ratio is 1:1. (1) The mortality and morbidity are primarily related to bleeding. Intracranial hemorrhage can be life threatening. The diagnosis is made at an early age, often during infancy because the clinical bleeding is severe in most patients with Factor XIII deficiency. Bleeding from the stump of the umbilical cord within the first days to weeks of life is a characteristic feature that occurs in 80% of affected individuals, bleeding from this specific site is uncommon in other inherited haemostatic diseases except afibrinogenemia. (2,3) Other clinical features include CNS hemorrhage (25-30%), Hemarthroses (20%), soft tissue bleeding and bruising. Recurrent spontaneous abortions are very common in women with FXIII deficiency, who do not receive FXIII replacement. (4,5) Delayed bleeding after trauma or surgery in pathognomic of FXIII deficiency. Wound healing is abnormal in a subset of patients. Although this child had features of Factor XIII deficiency since birth he was not diagnosed due to lack of facilities. Diagnosis is done by screening tests, functional assays, immunologic assays and genotyping. Appropriate imaging studies are required in the evaluation of suspected bleeding for instance CT scan in a patient with suspected CNS hemorrhage. Plasma, cryoprecipitate, and Factor XIII concentrates are used to treat bleeding in Factor XIII deficiency. The treatment of choice is plasma derived FXIII concentrate that is pasteurized to provide virologic safety and is less likely than plasma to cause systemic reactions (2) in our patient due to financial constraints we treated patient with fresh frozen plasma.

Prophylaxis is the management strategy of choice. Factor XIII concentrate 10-20U/kg every 4-6 weeks provides adequate plasma levels in most patients. (6) Genetic counseling and family studies should be part of a complete evaluation.

Contributors: AN collected the data and drafted the article and revised the manuscript for important intellectual content. He will act as guarantor of the study. UNR helped in manuscript writing.

Source of Funding: nil

Competing interests: nil
References :
  1. Anwar R, Miloszewski KJ. Factor XIII deficiency. Br J Haematol. 1999; 107: 468-484.
  2. Anwar R, Minford A, Gallivan L, Trinh CH, Markham AF. Delayed umbilical bleeding--a presenting feature for factor XIII deficiency: clinical features, genetics, and management. Pediatrics. 2002; 109: E32.
  3. Ariëns RA, Lai TS, Weisel JW, Greenberg CS, Grant PJ. Role of factor XIII in fibrin clot formation and effects of genetic polymorphisms. Blood. 2002; 100: 743-754.
  4. Ichinose A, Asahina T, Kobayashi T. Congenital blood coagulation factor XIII deficiency and perinatal management. Curr Drug Targ. 2005; 6: 541-549.
  5. 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: 235-238
  6. Nugent DJ. Prophylaxis in rare coagulation disorders -- factor XIII deficiency. Thromb Res. 2006;118: S23
Last Updated : Wednesday, September 01, 2010 Vol 7 Issue 9 Art #53
How to Cite URL :
Naseem A, Reddy N U. CONGENITAL FACTOR XIII DEFICIENCY. Pediatric Oncall [serial online] 2010[cited 2010 January 1];7. Art #53. Available From : http://www.pediatriconcall.com/Journal/Article/FullText.aspx?artid=330&type=J&tid=&imgid=&reportid=270&tbltype=
Disclaimer: The information given by www.pediatriconcall.com is provided by medical and paramedical & Health providers voluntarily for display & is meant only for informational purpose. The site does not guarantee the accuracy or authenticity of the information. Use of any information is solely at the user's own risk. The appearance of advertisement or product information in the various section in the website does not constitute an endorsement or approval by Pediatric Oncall of the quality or value of the said product or of claims made by its manufacturer.