Hereditary bleeding disorder, factor ix deficiency in females: a case series

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منابع مشابه

Hereditary bleeding disorder, factor ix deficiency in females: a case series

Introduction: Hemophilia is uncommon in females and there is little knowledge about the clinical

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Thrombosis in a bleeding disorder: case of thromboembolism in factor VII deficiency

Congenital factor VII deficiency (FVIID) is a rare disorder with a wide range of bleeding manifestations. The disorder does not protect patients against occurrence of thrombosis, and deep vein thrombosis can occur in the setting of surgery and recombinant factor VIIa replacement.

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Factor IX deficiency and bleeding in a patient with Sheehan's syndrome.

Factor IX deficiency was associated with a hemorrhagic disorder in a woman who previously had experienced postpartum hypotension resulting in Sheehan’s syndrome. There was no family history of Christmas disease, and other known causes of factor IX deficiency were excluded. Plasma levels of factor IX were partially corrected by therapy with thyroid hormones and completely restored to normal by t...

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Haemophilia B (Factor IX Deficiency)

If a woman is a carrier there is a 1 in 2 chance that any son will be affected and a 1 in 2 chance that any daughter will be a carrier. If a man with the disease fathers a child, any daughter will be a carrier and any son will be unaffected and will not carry the gene. There is a report of a daughter of a man with the disease who had a factor IX level of 5% and haemarthroses and this was though...

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Monocular Elevation Deficiency: A Case Series of Surgical Outcome

Background: Inferior rectus recession, Knapp procedure, partial tendon transposition, and combined procedure are different surgical procedures in the management of monocular elevation deficiency (MED). Only a few studies have been published on the management of this problem. In this study, we report our experience with patients with MED focusing on the indications and types of surgery in the so...

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ژورنال

عنوان ژورنال: Cases Journal

سال: 2009

ISSN: 1757-1626

DOI: 10.4076/1757-1626-2-8940