Factor X deficiency--a rare disorder.

Sangita Trivedi; Jurish Bhatia; Sumit Jain; Tushar H Toprani

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PubMed · 16295475

Factor X deficiency--a rare disorder.

Sangita Trivedi·Jurish Bhatia·Sumit Jain·Tushar H Toprani

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Abstract

Congenital factor X deficiency is a very rare inherited coagulation disorder. The clinical phenotype is of varying bleeding manifestations depending upon the level of factor activity. We describe a one and a half year old patient with severe deficiency (factor level less than 1%) who manifested with only easy bruisability and epistaxis that does not correlate with level of deficiency.

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Sangita Trivedi, Jurish Bhatia, Sumit Jain, Tushar H Toprani. 2004. Factor X deficiency--a rare disorder.. https://pubmed.ncbi.nlm.nih.gov/16295475/

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