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