Factor X Deficiency: A Rare Cause of Puberty Menorrhagia

Factor X deficiency is an extremely rare coagulation defect inherited as an autosomal recessive disorder with variable bleeding manifestations. The authors report case of a 16 y-old girl born from a consanguineous marriage who presented with excessive bleeding at the start of menarche. Investigation...

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Published inIndian journal of pediatrics Vol. 80; no. 7; pp. 607 - 608
Main Authors Singh, Virender, Kakkar, Tania, Digra, Sanjeev K., Kakkar, Manisha
Format Journal Article
LanguageEnglish
Published India Springer India 01.07.2013
Springer
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Summary:Factor X deficiency is an extremely rare coagulation defect inherited as an autosomal recessive disorder with variable bleeding manifestations. The authors report case of a 16 y-old girl born from a consanguineous marriage who presented with excessive bleeding at the start of menarche. Investigations revealed severe anemia, prolongation of both prothrombin time and activated partial thromboplastin time and moderate deficiency of factor X (1 %). She was given multiple transfusions including packed cells and fresh frozen plasma and was advised to remain under regular follow up.
Bibliography:ObjectType-Case Study-2
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ISSN:0019-5456
0973-7693
DOI:10.1007/s12098-012-0796-7