Gastrointestinal bleeding in a newborn infant with congenital factor X deficiency and COVID‐19—A common clinical feature between a rare disorder and a new, common infection

Author:

Dorgalaleh Akbar1ORCID,Baghaipour Mohammad Reza2,Tabibian Shadi12,Ghazizadeh Farid3,Dabbagh Ali4,Bahoush Gholamreza5,Jazebi Mohammad2,Bahraini Mehran1,Fazeli Alieh6ORCID,Baghaipour Nazanin2,Yousefi Forough7

Affiliation:

1. Department of Hematology and Blood Transfusion School of Allied Medicine Iran University of Medical Sciences Tehran Iran

2. Iranian Comprehensive hemophilia Care Center Tehran Iran

3. Department of Hematology Medical University of West Azarbaijan Iran

4. Anesthesia Department and Anesthesia Research Center Shahid Beheshti University of Medical Sciences Tehran Iran

5. Department of Pediatrics Aliasghar Children’s Hospital Iran University of Medical Science Tehran Iran

6. School of Paramedical Sciences Shiraz University of Medical Sciences Shiraz Iran

7. Department of Microbiology and Parasitology Faculty of Medicine Bushehr University of Medical Sciences Bushehr Iran

Publisher

Wiley

Subject

Biochemistry (medical),Clinical Biochemistry,Hematology,General Medicine

Reference10 articles.

1. Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene

2. Pharmacological management of rare coagulation factor deficiencies besides hemophilia

3. Bleeding and bleeding risk in COVID‐19;Dorgalaleh A;Semin Thromb Hemost,2020

4. Risk factors for disease severity, unimprovement, and mortality in COVID-19 patients in Wuhan, China

5. Patients with congenital bleeding disorders appear to be less severely affected by SARS‐ CoV‐2 ─ Inherited hypocoagulability overcoming acquired hypercoagulability of COVID‐19?;Dorgalaleh A;Semin Thromb Hemost,2020

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