Literature DB >> 46025

Adenosine-deaminase deficiency in a child diagnosed prenatally.

R Hirschhorn, N Beratis, F S Rosen, R Parkman, R Stern, S Polmar.   

Abstract

Deficiency of red-blood-cell adenosine deaminase (R.B.C.-A.D.A.) has been reported in a proportion of patients with the autosomal recessive form of severe combined immunodeficiency (S.C.I.D.). In a family in which a child had died with S.C.I.D., R.B.C.-A.D.A. levels in the parents and other members of the family were compatible with a heterozygous state for A.D.A. deficiency. Cultured amniotic-fluid cells obtained from a subsequent pregnancy contained less than 1.5% of A.D.A. activity of normal amniotic cultures. The prenatal diagnosis of A.D.A. deficiency was confirmed at birth by the absence of A.D.A. ACTIVITY IN THE CHILD'S RED-BLOOD-CELLS. Clinical and laboratory findings in this child are similar to those of the sibling who had died with S.C.I.D.

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Year:  1975        PMID: 46025     DOI: 10.1016/s0140-6736(75)91075-2

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  15 in total

1.  Adenosine deaminase activity in erythrocytes, lymphocytes, polymorphonuclear neutrophil leucocytes and cultured cells: a possible role in the immune response.

Authors:  A Adams; R A Harkness; J G McVie
Journal:  J Inherit Metab Dis       Date:  1978       Impact factor: 4.982

Review 2.  Short stature/short limb skeletal dysplasia with severe combined immunodeficiency and bowing of the femora: report of two patients and review.

Authors:  K D MacDermot; R M Winter; J S Wigglesworth; S Strobel
Journal:  J Med Genet       Date:  1991-01       Impact factor: 6.318

3.  Purine nucleoside metabolism in the erythrocytes of patients with adenosine deaminase deficiency and severe combined immunodeficiency.

Authors:  R P Agarwal; G W Crabtree; R E Parks; J A Nelson; R Keightley; R Parkman; F S Rosen; R C Stern; S H Polmar
Journal:  J Clin Invest       Date:  1976-04       Impact factor: 14.808

4.  Prenatal exclusion of purine nucleoside phosphorylase deficiency.

Authors:  E Carapella De Luca; M Stegagno; C Dionisi Vici; R Paesano; L D Fairbanks; G S Morris; H A Simmonds
Journal:  Eur J Pediatr       Date:  1986-04       Impact factor: 3.183

Review 5.  Combined immunodeficiency and inborn errors of purine metabolism.

Authors:  H J Meuwissen; B Pollara
Journal:  Blut       Date:  1978-10-13

6.  Early prenatal investigation of a pregnancy at risk of adenosine deaminase deficiency using chorionic villi.

Authors:  D A Aitken; D H Gilmore; C A Frew; M E Ferguson-Smith; M J Carty; W R Chatfield
Journal:  J Med Genet       Date:  1986-02       Impact factor: 6.318

Review 7.  The biochemical basis of immunodeficiency disease.

Authors:  K O Raivio
Journal:  Eur J Pediatr       Date:  1980-10       Impact factor: 3.183

8.  Conversion of human erythrocyte-adenosine deaminase activity to different tissue-specific isozymes. Evidence for a common catalytic unit.

Authors:  R Hirschhorn
Journal:  J Clin Invest       Date:  1975-03       Impact factor: 14.808

9.  Prenatal diagnosis for adenosine deaminase deficiency.

Authors:  J B Ziegler; M B Van der Weyden; C H Lee; A Daniel
Journal:  J Med Genet       Date:  1981-04       Impact factor: 6.318

10.  Prenatal diagnosis of three cases of severe combined immunodeficiency: severe T cell deficiency during the first half of gestation in fetuses with adenosine deaminase deficiency.

Authors:  D C Linch; R J Levinsky; C H Rodeck; K A Maclennan; H A Simmonds
Journal:  Clin Exp Immunol       Date:  1984-05       Impact factor: 4.330

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