Literature DB >> 25536973

The classic and nonclassic concenital adrenal hyperplasias.

Richard J Auchus.   

Abstract

OBJECTIVE: The American Association of Clinical Endocrinologists Adrenal Scientific Committee has developed a series of articles to update members on the genetics of adrenal diseases.
METHODS: Case presentation, discussion of literature, table, and bullet point conclusions.
RESULTS: The congenital adrenal hyperplasia (CAH) syndromes are autosomal recessive defects in cortisol biosynthesis. The phenotype of each CAH patient depends on the defective enzyme and the severity of the defect. Clinical manifestations derive from both failure to synthesize hormones distal to the enzymatic block, as well as consequences from cortisol precursor accumulation proximal to the block, often with diversion to other biologically active steroids. The most common form of CAH is 21-hydroxylase deficiency, which occurs in the classic form in 1 in 16,000 newborns and in a milder or nonclassic form in at least 1 in 1,000 people.
CONCLUSION: This article reviews the various forms of CAH and pitfalls in the diagnosis and treatment of these conditions.

Entities:  

Mesh:

Year:  2014        PMID: 25536973     DOI: 10.4158/EP14474.RA

Source DB:  PubMed          Journal:  Endocr Pract        ISSN: 1530-891X            Impact factor:   3.443


  8 in total

1.  Trophoblast Retrieval and Isolation From the Cervix for Noninvasive, First Trimester, Fetal Gender Determination in a Carrier of Congenital Adrenal Hyperplasia.

Authors:  Alan D Bolnick; Rani Fritz; Chandni Jain; Leena Kadam; Jay M Bolnick; Brian A Kilburn; Manvinder Singh; Michael P Diamond; Sascha Drewlo; D Randall Armant
Journal:  Reprod Sci       Date:  2016-02-25       Impact factor: 3.060

Review 2.  The hunt for a selective 17,20 lyase inhibitor; learning lessons from nature.

Authors:  Ian M Bird; David H Abbott
Journal:  J Steroid Biochem Mol Biol       Date:  2016-05-03       Impact factor: 4.292

3.  Clinical significance of 11-oxygenated androgens.

Authors:  Adina F Turcu; Richard J Auchus
Journal:  Curr Opin Endocrinol Diabetes Obes       Date:  2017-06       Impact factor: 3.243

Review 4.  Steroid biomarkers in human adrenal disease.

Authors:  Juilee Rege; Adina F Turcu; Tobias Else; Richard J Auchus; William E Rainey
Journal:  J Steroid Biochem Mol Biol       Date:  2019-01-29       Impact factor: 4.292

Review 5.  Non-Classical Congenital Adrenal Hyperplasia in Childhood.

Authors:  Selim Kurtoğlu; Nihal Hatipoğlu
Journal:  J Clin Res Pediatr Endocrinol       Date:  2016-06-29

6.  Phenotypic Variation of 46,XX Late Identified Congenital Adrenal Hyperplasia among Indonesians.

Authors:  Achmad Zulfa Juniarto; Maria Ulfah; Mahayu Dewi Ariani; Agustini Utari; Sultana Mh Faradz
Journal:  J ASEAN Fed Endocr Soc       Date:  2018-03-12

7.  Abiraterone acetate treatment lowers 11-oxygenated androgens.

Authors:  Connor Wright; Patrick O'Day; Mohammed Alyamani; Nima Sharifi; Richard J Auchus
Journal:  Eur J Endocrinol       Date:  2020-04       Impact factor: 6.664

8.  Classical 11β-Hydroxylase Deficiency Caused by a Novel Homozygous Mutation: A Case Study and Literature Review.

Authors:  Mohammad N Alsanea; Abdulmoein Al-Agha; Mohamed Abdelmaksoud Shazly
Journal:  Cureus       Date:  2022-01-23
  8 in total

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