ro13-9904 and Agammaglobulinemia

ro13-9904 has been researched along with Agammaglobulinemia* in 2 studies

Other Studies

2 other study(ies) available for ro13-9904 and Agammaglobulinemia

Article	Year
Massive empyema associated with transient hypogammaglobulinemia of infancy and IgA deficiency. Journal of Korean medical science, 2009, Volume: 24, Issue:2 Transient hypogammaglobulinemia of infancy (THI) is originally defined as a physiological maturation defect of immunoglobulin G (IgG) production that occurs at 3-6 months of age and lasts until 18 to 36 months of age. We report here on a 22-month-old child with THI and IgA deficiency, who had massive pneumococcal empyema. Her depressed IgG level returned to normal within 6 months, but IgA level was still low at 6 yr of age. Although THI is an age-dependent and self-limiting disorder, severe infection that includes an atypical presentation of an infection may occur in some patients and this requires evaluation with immunologic study. Topics: Agammaglobulinemia; Anti-Bacterial Agents; Ceftriaxone; Drug Resistance, Bacterial; Empyema, Pleural; Female; Humans; IgA Deficiency; Immunoglobulin A; Immunoglobulin G; Infant; Staphylococcal Infections; Tomography, X-Ray Computed	2009
Drug reaction to ceftriaxone in a child with X-linked agammaglobulinemia. The Journal of allergy and clinical immunology, 2002, Volume: 109, Issue:5 Topics: Agammaglobulinemia; Ceftriaxone; Cephalosporins; Child, Preschool; Drug Eruptions; Genetic Linkage; Humans; Male; X Chromosome	2002

Article

Year

Massive empyema associated with transient hypogammaglobulinemia of infancy and IgA deficiency.

Journal of Korean medical science, 2009, Volume: 24, Issue:2

Transient hypogammaglobulinemia of infancy (THI) is originally defined as a physiological maturation defect of immunoglobulin G (IgG) production that occurs at 3-6 months of age and lasts until 18 to 36 months of age. We report here on a 22-month-old child with THI and IgA deficiency, who had massive pneumococcal empyema. Her depressed IgG level returned to normal within 6 months, but IgA level was still low at 6 yr of age. Although THI is an age-dependent and self-limiting disorder, severe infection that includes an atypical presentation of an infection may occur in some patients and this requires evaluation with immunologic study.

Topics: Agammaglobulinemia; Anti-Bacterial Agents; Ceftriaxone; Drug Resistance, Bacterial; Empyema, Pleural; Female; Humans; IgA Deficiency; Immunoglobulin A; Immunoglobulin G; Infant; Staphylococcal Infections; Tomography, X-Ray Computed

2009

Drug reaction to ceftriaxone in a child with X-linked agammaglobulinemia.

The Journal of allergy and clinical immunology, 2002, Volume: 109, Issue:5

Topics: Agammaglobulinemia; Ceftriaxone; Cephalosporins; Child, Preschool; Drug Eruptions; Genetic Linkage; Humans; Male; X Chromosome

2002