Literature DB >> 218988

"Acquired" adrenal hyperplasia with 21-hydroxylase deficiency is not the same genetic disorders as congenital adrenal hyperplasia.

M I New, F Lorenzen, S Pang, P Gunczler, B Dupont, L S Levine.   

Abstract

Hormonal studies and HLA genotyping were performed on the family of a patient with "acquired" adrenal hyperplasia (AAH) due to 21-hydroxylase deficiency. The results of these studies suggest that "AAH", is not the same genetic disease as CAH.

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Year:  1979        PMID： 218988     DOI： 10.1210/jcem-48-2-356

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN： 0021-972X            Impact factor:   5.958


  11 in total

1.  Neonatal screening programme for congenital adrenal hyperplasia in a homogeneous Caucasian population.

Authors:  E Cacciari; A Balsamo; A Cassio; S Piazzi; F Bernardi; S Salardi; A Cicognani; P Pirazzoli; F Zappulla; M Capelli
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

2.  A segregation and linkage study of classical and nonclassical 21-hydroxylase deficiency.

Authors:  S L Sherman; C E Aston; N E Morton; P W Speiser; M I New
Journal:  Am J Hum Genet       Date:  1988-06       Impact factor: 11.025

Review 3.  Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a review of current knowledge.

Authors:  G E Bacon; R P Kelch
Journal:  J Endocrinol Invest       Date:  1979 Jan-Mar       Impact factor: 4.256

4.  Steroid disorders in children: congenital adrenal hyperplasia and apparent mineralocorticoid excess.

Authors:  M I New; R C Wilson
Journal:  Proc Natl Acad Sci U S A       Date:  1999-10-26       Impact factor: 11.205

5.  Neonatal screening for congenital adrenal hyperplasia.

Authors:  E Cacciari; A Balsamo; A Cassio; S Piazzi; F Bernardi; S Salardi; A Cicognani; P Pirazzoli; F Zappulla; M Capelli
Journal:  Arch Dis Child       Date:  1983-10       Impact factor: 3.791

6.  Increase of lymphocytic H-Y antigen in female 21-hydroxylase deficiency.

Authors:  V Amice; J Amice; J P Bercovici; R Fauchet
Journal:  Experientia       Date:  1984-03-15

7.  HLA and hormonal studies in 5 patients with late-onset 21-hydroxylase deficiency syndrome (21OHDS).

Authors:  C Scaroni; E Orlandini; C Venturi Pasini; M Gangemi; F Mantero
Journal:  J Endocrinol Invest       Date:  1986-02       Impact factor: 4.256

8.  Detection of late onset steroid 21-hydroxylase deficiency by capillary gas chromatographic profiling of urinary steroids in children and adolescents.

Authors:  J Homoki; J Solyom; W M Teller
Journal:  Eur J Pediatr       Date:  1988-04       Impact factor: 3.183

9.  HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiency.

Authors:  M S Pollack; L S Levine; G J O'Neill; S Pang; F Lorenzen; B Kohn; G F Rondanini; G Chiumello; M I New; B Dupont
Journal:  Am J Hum Genet       Date:  1981-07       Impact factor: 11.025

10.  Association of certain human leukocyte antigens with nephropathic cystinosis in the absence of linkage between these loci.

Authors:  R Steinherz; D Raiford; K K Mittal; J D Schulman
Journal:  Am J Hum Genet       Date:  1981-03       Impact factor: 11.025
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