Congenital factor II deficiency

An inherited bleeding disorder due to reduced activity of factor II (FII, prothrombin) and characterized by mucocutaneous bleeding symptoms.

Anemia

A reduction in erythrocytes volume or hemoglobin concentration.


Total: 2

                       


(per page)
PMID (PMCID)
20608021
 MIXED_SAMPLE
Budd-Chiari syndrome.
Bane A, Kebede D.
Ethiop Med J. 2010;48(2):169-75.
A 16-year-old Ethiopian male patient presented with 18 months history of anasarca, anemia & hepatomegaly associated with hypoprothrombinemia, and diagnosed to have Budd-Chiari syndrome (BCS).
1036036
 MALE Infant, Newborn
[Intracranial hemorrhage in an infant due to vitamin K deficiency --successful management of spontaneous intracerebral and subjural hematoma].
Shirai S, Owada M, Fujita Y, Akimoto M, Hayashi M.
No To Shinkei. 1976;28(12):1359-64.
The blood studies showed anemia and hypoprothrombinemia.