Literature DB >> 6327799

The endocrine pattern of late onset adrenal hyperplasia (21-hydroxylase deficiency).

E Carmina, A M Gagliano, F Rosato, M Maggiore, A Jannì.   

Abstract

We describe 5 adult women with severe hirsutism due to late onset 21-hydroxylase deficiency. Diagnosis was performed on the finding of high serum 17-hydroxyprogesterone (17OHP) levels with a marked hyperresponse to an ACTH test. The endocrine study showed in most patients a gonadotropin behavior similar to that observed in classical polycystic ovary (PCO) syndrome. Prolactin levels were slightly increased in basal conditions and presented an exaggerated response to TRH stimulation.

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Year:  1984        PMID： 6327799     DOI： 10.1007/BF03348395

Source DB:  PubMed          Journal:  J Endocrinol Invest        ISSN： 0391-4097            Impact factor:   4.256


  13 in total

1.  Early adrenal response to ACTH; Plasma concentrations of pregnenolone, 17-hydroxypregnenolone, progesterone, and 17-hydroxyprogesterone.

Authors:  J A Bermudez; M B Lipsett
Journal:  J Clin Endocrinol Metab       Date:  1972-01       Impact factor: 5.958

2.  Congenital adrenal hyperplasia due to partial 21-hydroxylase deficiency. A study of five cases.

Authors:  P Bouchard; F Kuttenn; I Mowszowicz; G Schaison; M C Raux-Eurin; P Mauvais-Jarvis
Journal:  Acta Endocrinol (Copenh)       Date:  1981-01

3.  Pubertal presentation of congenital delta 5-3 beta-hydroxysteroid dehydrogenase deficiency.

Authors:  R L Rosenfield; B H Rich; J I Wolfsdorf; F Cassorla; J S Parks; A M Bongiovanni; C H Wu; C H Shackleton
Journal:  J Clin Endocrinol Metab       Date:  1980-08       Impact factor: 5.958

4.  An attenuated form of congenital virilizing adrenal hyperplasia.

Authors:  Z Rosenwaks; P A Lee; G S Jones; C J Migeon; A C Wentz
Journal:  J Clin Endocrinol Metab       Date:  1979-09       Impact factor: 5.958

5.  Late-onset 21-hydroxylase deficiency mimicking idiopathic hirsutism or polycystic ovarian disease.

Authors:  G P Chrousos; D L Loriaux; D L Mann; G B Cutler
Journal:  Ann Intern Med       Date:  1982-02       Impact factor: 25.391

6.  Adult manifestation of congenital adrenal hyperplasia due to incomplete 21-hydroxylase deficiency mimicking polycystic ovarian disease.

Authors:  R A Lobo; U Goebelsmann
Journal:  Am J Obstet Gynecol       Date:  1980-11-15       Impact factor: 8.661

7.  Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia.

Authors:  B Kohn; L S Levine; M S Pollack; S Pang; F Lorenzen; D Levy; A J Lerner; G F Rondanini; B Dupont; M I New
Journal:  J Clin Endocrinol Metab       Date:  1982-11       Impact factor: 5.958

8.  Attenuated forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Authors:  P A Lee; Z Rosenwaks; M D Urban; C J Migeon; W D Bias
Journal:  J Clin Endocrinol Metab       Date:  1982-11       Impact factor: 5.958

9.  Adrenocortical 11 beta-hydroxylation defect in adult women with postmenarchial onset of symptoms.

Authors:  G Cathelineau; J L Brerault; J Fiet; R Julien; C Dreux; J Canivet
Journal:  J Clin Endocrinol Metab       Date:  1980-08       Impact factor: 5.958

10.  Clinical aspects of the polycystic ovary syndrome.

Authors:  S G Raj; I E Thompson; M J Berger; M L Taymor
Journal:  Obstet Gynecol       Date:  1977-05       Impact factor: 7.661
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  2 in total

1.  New reliable biochemical marker for screening 21 alpha-hydroxylase deficiency without index person among hirsute women in agreement with HLA-haplotyping.

Authors:  A Chryssikopoulos; I Phocas; A Sarandakou; E Trakakis; D Rizos
Journal:  J Endocrinol Invest       Date:  1995-11       Impact factor: 4.256

2.  Increased DHEAs levels in PCO syndrome: evidence for the existence of two subgroups of patients.

Authors:  E Carmina; F Rosato; A Jannì
Journal:  J Endocrinol Invest       Date:  1986-02       Impact factor: 4.256
  2 in total

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