Homozygous protein S deficiency in an infant with purpura fulminans.

Mahasandana, C; Suvatte, V; Chuansumrit, A; Marlar, R A; Manco-Johnson, M J; Jacobson, L J; Hathaway, W E

Mahasandana, C; Suvatte, V; Chuansumrit, A; Marlar, R A; Manco-Johnson, M J; Jacobson, L J; Hathaway, W E.

Affiliation

Mahasandana C; Department of Pediatrics, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand.

J Pediatr ; 117(5): 750-3, 1990 Nov.

Article in En | MEDLINE | ID: mdl-2231208

Subject(s)

Complement Inactivator Proteins; Glycoproteins; Protein Deficiency/complications; Purpura/etiology; Adult; Age Factors; Blood Coagulation Tests; Blood Proteins/analysis; Carrier Proteins/analysis; Female; Homozygote; Humans; Immunoelectrophoresis, Two-Dimensional; Infant, Newborn; Male; Protein C/analysis; Protein Deficiency/blood; Protein Deficiency/genetics; Purpura/blood; Purpura/drug therapy; Warfarin/therapeutic use

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Collection: 01-internacional Database: MEDLINE Main subject: Protein Deficiency / Purpura / Complement Inactivator Proteins / Glycoproteins Limits: Adult / Female / Humans / Male / Newborn Language: En Journal: J Pediatr Year: 1990 Document type: Article Affiliation country: Thailand Country of publication: United States

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