Literature DB >> 5019089

Diagnosis of immunologic deficiency in childhood.

P J Edelson.   

Abstract

A defective host response may be responsible for recurring infections in certain children. Recognition of these defects may be important both therapeutically for the patient and for genetic counseling for the family. Family history, age of onset of illness and type of infecting agents may all point to one or another defect in host resistance. An initial evaluation for suspected immunologic disease may be rapidly accomplished and should include absolute neutrophil and lymphocyte counts, chest X-ray for a thymic shadow, Schick test for functional IgG antibodies and isohemagglutinin titers for functional IgM antibodies. Although serum protein electrophoresis is unreliable for diagnosis of most disorders of circulating antibodies, quantitation of the IgG, IgA and IgM antibody classes is generally available. More extensive studies may be carried out to further define defects in the cell-mediated immune system, in the various complement components, or in the ingestion and killing of bacteria by neutrophils.

Entities:  

Mesh:

Substances:

Year:  1972        PMID: 5019089      PMCID: PMC1518345     

Source DB:  PubMed          Journal:  Calif Med        ISSN: 0008-1264


  9 in total

Review 1.  THE PATHOGENESIS OF IMMUNOLOGIC DEFICIENCY DISEASES.

Authors:  R D PETERSON; M D COOPER; R A GOOD
Journal:  Am J Med       Date:  1965-04       Impact factor: 4.965

2.  Agammaglobulinemia.

Authors:  O C BRUTON
Journal:  Pediatrics       Date:  1952-06       Impact factor: 7.124

3.  Phytohaemagglutinin unresponsiveness of lymphocytes from babies with congenital rubella.

Authors:  G B Olson; M A South; R A Good
Journal:  Nature       Date:  1967-05-13       Impact factor: 49.962

Review 4.  Analytic review: disorders of phagocyte function.

Authors:  S D Douglas
Journal:  Blood       Date:  1970-06       Impact factor: 22.113

Review 5.  Thymic dysplasia. A separable entity from "swiss agammaglobulinemia".

Authors:  M E Miller; R M Schieken
Journal:  Am J Med Sci       Date:  1967-06       Impact factor: 2.378

6.  Hereditary lymphopenic agammaglobulinemia associated with a distinctive form of short-limbed dwarfism and ectodermal dysplasia.

Authors:  R A Gatti; N Platt; H H Pomerance; R Hong; L O Langer; H E Kay; R A Good
Journal:  J Pediatr       Date:  1969-10       Impact factor: 4.406

7.  In vitro bactericidal capacity of human polymorphonuclear leukocytes: diminished activity in chronic granulomatous disease of childhood.

Authors:  P G Quie; J G White; B Holmes; R A Good
Journal:  J Clin Invest       Date:  1967-04       Impact factor: 14.808

8.  Chediak-Higashi syndrome: hereditary gigantism of cytoplasmic organelles.

Authors:  D B Windhorst; A S Zelickson; R A Good
Journal:  Science       Date:  1966-01-07       Impact factor: 47.728

9.  Wiskott-Aldrich syndrome, a genetically determined cellular immunologic deficiency: clinical and laboratory responses to therapy with transfer factor.

Authors:  A S Levin; L E Spitler; D P Stites; H H Fudenberg
Journal:  Proc Natl Acad Sci U S A       Date:  1970-10       Impact factor: 11.205

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.