Document Detail


Factor X deficiency--a rare disorder.
MedLine Citation:
PMID:  16295475     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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.
Authors:
Sangita Trivedi; Jurish Bhatia; Sumit Jain; Tushar H Toprani
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Indian journal of pathology & microbiology     Volume:  47     ISSN:  0377-4929     ISO Abbreviation:  Indian J Pathol Microbiol     Publication Date:  2004 Apr 
Date Detail:
Created Date:  2005-11-18     Completed Date:  2005-12-23     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  7605904     Medline TA:  Indian J Pathol Microbiol     Country:  India    
Other Details:
Languages:  eng     Pagination:  223-4     Citation Subset:  IM    
Affiliation:
Department of Pathology, KGP Children Hospital and Jajodia Research Institute, Karelibaug, Vadodara. sangita_trivedi@hotmail.com
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MeSH Terms
Descriptor/Qualifier:
Blood Coagulation Tests
Factor X Deficiency / blood,  congenital*,  diagnosis
Humans
Infant
Male
Phenotype

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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