Literature DB >> 3794886

Transient hypogammaglobulinemia of infancy: need to reconsider name and definition.

S J McGeady.   

Abstract

Twenty-three infants with diminished levels of one or more immunoglobulin isotypes, intact antibody producing capacity, and a generally benign clinical course were initially diagnosed as having transient hypogammaglobulinemia of infancy. Prospective evaluation of these infants, including seven to age 60 months, revealed that acquisition of normal immunoglobulin levels was often delayed beyond infancy. In some cases the diminished immunoglobulin levels were a prodrome of selective lgA deficiency. These children seemed to experience frequent sinopulmonary infections early in life, but fewer with age. None of these children received exogenous gammaglobulin. The designation of transient hypogammaglobulinemia of infancy is a misnomer, and the diagnosis, even if accepted, can be made only in retrospect. The alternative designation hypogammaglobulinemia of early childhood is suggested, to which can be added "with recovery" or "with development of other dysgammaglobulinemia," depending on the eventual phenotype observed.

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Year:  1987        PMID: 3794886     DOI: 10.1016/s0022-3476(87)80286-x

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  12 in total

1.  Infants presenting with recurrent infections and low immunoglobulins: characteristics and analysis of normalization.

Authors:  M A Whelan; W H Hwan; J Beausoleil; W W Hauck; S J McGeady
Journal:  J Clin Immunol       Date:  2006-01       Impact factor: 8.317

Review 2.  Study of patients with Hyper-IgM type IV phenotype who recovered spontaneously during late childhood and review of the literature.

Authors:  Neslihan Edeer Karaca; Anne Durandy; Nesrin Gulez; Guzide Aksu; Necil Kutukculer
Journal:  Eur J Pediatr       Date:  2011-01-28       Impact factor: 3.183

3.  Phenotypic parameters predict time to normalization in infants with hypogammaglobulinemia.

Authors:  Robert C Van Winkle; Walter W Hauck; Stephen J McGeady
Journal:  J Clin Immunol       Date:  2013-09-08       Impact factor: 8.317

Review 4.  Pathogenesis, diagnosis, and management of primary antibody deficiencies and infections.

Authors:  Ari J Fried; Francisco A Bonilla
Journal:  Clin Microbiol Rev       Date:  2009-07       Impact factor: 26.132

5.  Immunodeficiency due to a unique protracted developmental delay in the B-cell lineage.

Authors:  A S Goldman; S E Miles; H E Rudloff; K H Palkowetz; F C Schmalstieg
Journal:  Clin Diagn Lab Immunol       Date:  1999-03

6.  Transient hypogammaglobulinaemia of infancy: many patients recover in adolescence and adulthood.

Authors:  R Ameratunga; Y Ahn; R Steele; S-T Woon
Journal:  Clin Exp Immunol       Date:  2019-07-22       Impact factor: 4.330

7.  Recognizing primary immune deficiency in clinical practice.

Authors:  Hale Yarmohammadi; Lissette Estrella; John Doucette; Charlotte Cunningham-Rundles
Journal:  Clin Vaccine Immunol       Date:  2006-03

8.  Features of transient hypogammaglobulinaemia in infants screened for immunological abnormalities.

Authors:  A M Walker; A S Kemp; D J Hill; M J Shelton
Journal:  Arch Dis Child       Date:  1994-03       Impact factor: 3.791

9.  Approach to the child with recurrent infections.

Authors:  Suzan A Alkhater
Journal:  J Family Community Med       Date:  2009-09

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

Authors:  Kuhn Park; Kyung-Yil Lee; Mi-Hee Lee; Joon-Sung Lee; Ji-Chang Kim
Journal:  J Korean Med Sci       Date:  2009-04-20       Impact factor: 2.153

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