Literature DB >> 1096976

T-cell deficiency in diGeorge syndrome.

H W Lischner, D S Huff.   

Abstract

DiGeorge syndrome is broadly defined as absence or hypoplasia of the thymus due to dysmorphogenesis of the third and fourth pharyngeal pouches in early embryonic life. Various tests of thymic function have been evaluated in some 19 infants and young children with this syndrome. Deficiency of T lymphocytes has been shown to occur in the presence of as much as 10 to 20% of the normal amount of histologically normal thymic tissue in the partial DiGeorge syndrome.

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Year:  1975        PMID: 1096976

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN: 0547-6844


  5 in total

1.  Longitudinal analysis of lymphocyte function and numbers in the first year of life in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

Authors:  K E Sullivan; D McDonald-McGinn; D A Driscoll; B S Emanuel; E H Zackai; A F Jawad
Journal:  Clin Diagn Lab Immunol       Date:  1999-11

2.  Impaired T8 lymphocyte-mediated suppressive activity in patients with partial Di George syndrome.

Authors:  A Durandy; F Le Deist; A Fischer; C Griscelli
Journal:  J Clin Immunol       Date:  1986-05       Impact factor: 8.317

Review 3.  DiGeorge syndrome/chromosome 22q11.2 deletion syndrome.

Authors:  K E Sullivan
Journal:  Curr Allergy Asthma Rep       Date:  2001-09       Impact factor: 4.806

4.  Age-related gene expression in Tourette syndrome.

Authors:  Lisa Lit; Amanda Enstrom; Frank R Sharp; Donald L Gilbert
Journal:  J Psychiatr Res       Date:  2008-05-15       Impact factor: 4.791

5.  DiGeorge syndrome with hypogammaglobulinaemia: a patient with excess suppressor T cell activity treated with fetal thymus transplantation.

Authors:  M Mayumi; H Kimata; Y Suehiro; S Hosoi; S Ito; Y Kuge; K Shinomiya; H Mikawa
Journal:  Eur J Pediatr       Date:  1989-04       Impact factor: 3.183

  5 in total

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