Document Detail


Management of neonatal purpura fulminans with severe protein C deficiency.
MedLine Citation:
PMID:  16820665     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Neonatal purpura fulminans is a life threatening clinical entity characterized by extensive subcutaneous thrombosis and disseminated intravascular coagulation usually manifesting shortly after birth. We report an autosomal recessive form of the disease in a neonate who was diagnosed with compound heterozygosity for mutations in his protein C gene as the molecular basis of his disorder.
Authors:
Krishna Sen; Angshumoy Roy
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Indian pediatrics     Volume:  43     ISSN:  0019-6061     ISO Abbreviation:  Indian Pediatr     Publication Date:  2006 Jun 
Date Detail:
Created Date:  2006-07-05     Completed Date:  2006-09-12     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  2985062R     Medline TA:  Indian Pediatr     Country:  India    
Other Details:
Languages:  eng     Pagination:  542-5     Citation Subset:  IM    
Affiliation:
Department of Pediatric Medicine, Park Childrens Center for Treatment and Research, 4 Gorky Terrace, Kolkata 700 019, India. dockrishnasen@gmail.com
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MeSH Terms
Descriptor/Qualifier:
Anticoagulants / therapeutic use*
Humans
Infant, Newborn
Male
Mutation
Protein C / therapeutic use*
Protein C Deficiency / complications*,  genetics
Purpura, Schoenlein-Henoch / complications,  drug therapy*
Risk Assessment
Thrombophilia / etiology*
Chemical
Reg. No./Substance:
0/Anticoagulants; 0/Protein C

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


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