Hemophilia B

Hemophilia B is a form of hemophilia (see this term) characterized by spontaneous or prolonged hemorrhages due to factor IX deficiency.

Splenic rupture

A breach of the capsule of the spleen.


Total: 2

                       


(per page)
PMID (PMCID)
16952601
 MALE
Nonoperative management of delayed splenic rupture in a patient with hemophilia B.
Terry NE, Boswell WC.
J Pediatr Surg. 2006;41(9):1607-9.
Nonoperative management of delayed splenic rupture in a patient with hemophilia B.
7301394
 MALE Child
[Biphasic splenic rupture in a hemophilic child (author's transl)].
Kaulfersch W, Hollwarth M, Muntean W.
Padiatr Padol. 1981;16(4):465-7.
This report describes a biphasic splenic rupture following trauma in a 12 1/2 years old boy with the severe form of hemophilia B.