Your browser doesn't support javascript.
loading
Aplastic crisis due to human parvovirus B19 infection in hereditary hemolytic anaemia
Cubel, R. C. N; Valadäo, M. C; Pereira, W. V; Magalhäes, M. C; Nascimento, J. P.
Rev. Inst. Med. Trop. Säo Paulo ; Rev. Inst. Med. Trop. Säo Paulo;34(5): 479-82, set.-out. 1992. tab
Article in En | LILACS | ID: lil-134549
Responsible library: BR66.1
RESUMO
Specific anti-B19 IgM was demonstrated in sera from three children showing transient aplastic crisis. A two years-old boy living in Rio de Janeiro suffering from sickle-cell anaemia showed the crisis during August, 1990. Two siblings living in Santa Maria, RS, developed aplastic crisis during May, 1991, when they were also diagnosed for hereditary spherocytosis. For a third child from this same family, who first developed aplastic crisis no IgM anti-B19 was detected in her sera
Subject(s)
Fulltext
Add to My VHL
Print
XML
Search on Google
Full text: 1 Collection: 01-internacional Database: LILACS Main subject: Spherocytosis, Hereditary / Erythema Infectiosum / Anemia, Aplastic / Anemia, Sickle Cell Type of study: Diagnostic_studies Limits: Female / Humans / Male Language: En Journal: Rev. Inst. Med. Trop. Säo Paulo Journal subject: MEDICINA TROPICAL Year: 1992 Document type: Article Country of publication: Brazil
Fulltext
Add to My VHL
Print
XML
Search on Google
Full text: 1 Collection: 01-internacional Database: LILACS Main subject: Spherocytosis, Hereditary / Erythema Infectiosum / Anemia, Aplastic / Anemia, Sickle Cell Type of study: Diagnostic_studies Limits: Female / Humans / Male Language: En Journal: Rev. Inst. Med. Trop. Säo Paulo Journal subject: MEDICINA TROPICAL Year: 1992 Document type: Article Country of publication: Brazil