Literature DB >> 26047556

The next 150 years of congenital adrenal hyperplasia.

Adina F Turcu1, Richard J Auchus2.   

Abstract

Congenital adrenal hyperplasias (CAH) are a group of autosomal recessive defects in cortisol biosynthesis. Substantial progress has been made since the description of the first report, 150 years ago. This article reviews some of the recent advances in the genetics, diagnosis and treatment of CAH. In addition, we underline the aspects where further progress is required, including, among others, better diagnostic modalities for the mild phenotype and for some of the rare forms of disease, elucidation of epigenetic factors that lead to different phenotypes in patients with identical genotype and expending on treatment options for controlling the adrenal androgen excess.
Copyright © 2015 Elsevier Ltd. All rights reserved.

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Year:  2015        PMID: 26047556      PMCID: PMC4568140          DOI: 10.1016/j.jsbmb.2015.05.013

Source DB:  PubMed          Journal:  J Steroid Biochem Mol Biol        ISSN: 0960-0760            Impact factor:   4.292


  134 in total

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Authors:  Kristina A Strnadová; Felix Votava; Jan Lebl; Adolf Mühl; Chike Item; Olaf A Bodamer; Toni Torresani; Ivan Bouska; Franz Waldhauser; Wolfgang Sperl
Journal:  Eur J Pediatr       Date:  2006-09-22       Impact factor: 3.183

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Journal:  J Clin Invest       Date:  1991-05       Impact factor: 14.808

6.  Deletion of amino acids Asp487-Ser488-Phe489 in human cytochrome P450c17 causes severe 17 alpha-hydroxylase deficiency.

Authors:  C E Fardella; L H Zhang; P Mahachoklertwattana; D Lin; W L Miller
Journal:  J Clin Endocrinol Metab       Date:  1993-08       Impact factor: 5.958

7.  Male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency.

Authors:  M I New
Journal:  J Clin Invest       Date:  1970-10       Impact factor: 14.808

8.  Detection and functional characterization of the novel missense mutation Y254D in type II 3 beta-hydroxysteroid dehydrogenase (3 beta HSD) gene of a female patient with nonsalt-losing 3 beta HSD deficiency.

Authors:  R Sanchez; E Rhéaume; N Laflamme; R L Rosenfield; F Labrie; J Simard
Journal:  J Clin Endocrinol Metab       Date:  1994-03       Impact factor: 5.958

9.  Newly proposed hormonal criteria via genotypic proof for type II 3beta-hydroxysteroid dehydrogenase deficiency.

Authors:  Chantal Lutfallah; Weihua Wang; J Ian Mason; Ying Tai Chang; Anzar Haider; Barry Rich; Mariano Castro-Magana; Kenneth C Copeland; Raphael David; Songya Pang
Journal:  J Clin Endocrinol Metab       Date:  2002-06       Impact factor: 5.958

10.  High reliability of neonatal screening for congenital adrenal hyperplasia in Switzerland.

Authors:  Michael Steigert; Eugen J Schoenle; Anna Biason-Lauber; Toni Torresani
Journal:  J Clin Endocrinol Metab       Date:  2002-09       Impact factor: 5.958

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  13 in total

1.  A novel splice site variant in CYP11A1 in trans with the p.E314K variant in a male patient with congenital adrenal insufficiency.

Authors:  Montserrat Lara-Velazquez; Alexander Perdomo-Pantoja; Patrick R Blackburn; Jennifer M Gass; Thomas R Caulfield; Paldeep S Atwal
Journal:  Mol Genet Genomic Med       Date:  2017-07-20       Impact factor: 2.183

2.  46,XY Disorder of Sex Development Caused by 17α-Hydroxylase/17,20-Lyase Deficiency due to Homozygous Mutation of CYP17A1 Gene: Consequences of Late Diagnosis.

Authors:  Giampaolo Papi; Rosa Maria Paragliola; Paola Concolino; Carlo Di Donato; Alfredo Pontecorvi; Salvatore Maria Corsello
Journal:  Case Rep Endocrinol       Date:  2018-04-24

3.  Newborn screening for congenital adrenal hyperplasia in New York State.

Authors:  Melissa Pearce; Lenore DeMartino; Rebecca McMahon; Rhonda Hamel; Breanne Maloney; Daniele-Marisa Stansfield; Emily C McGrath; Amanda Occhionero; Adam Gearhart; Michele Caggana; Norma P Tavakoli
Journal:  Mol Genet Metab Rep       Date:  2016-03-12

4.  17α‑hydroxylase/17,20‑lyase deficiency in congenital adrenal hyperplasia: A case report.

Authors:  Simiao Xu; Shuhong Hu; Xuefeng Yu; Muxun Zhang; Yan Yang
Journal:  Mol Med Rep       Date:  2016-12-12       Impact factor: 2.952

5.  Giant bilateral adrenal myelolipomas in two Chinese families with congenital adrenal hyperplasia.

Authors:  Qiuli Liu; Lin-Ang Wang; Jian Su; Dali Tong; Weihua Lan; Luofu Wang; Gaolei Liu; Jun Zhang; Victor Wei Zhang; Dianzheng Zhang; Rongrong Chen; Qingyi Zhu; Jun Jiang
Journal:  Endocr Connect       Date:  2018-09-01       Impact factor: 3.335

Review 6.  The human adrenal cortex: growth control and disorders.

Authors:  Claudimara Ferini Pacicco Lotfi; Jean Lucas Kremer; Barbara Dos Santos Passaia; Isadora Pontes Cavalcante
Journal:  Clinics (Sao Paulo)       Date:  2018-09-06       Impact factor: 2.365

7.  A Rare Case of Hypertension in a Young (Fe)male.

Authors:  Anvesh Golla; Sreebhushan Raju; Krishna Prasad
Journal:  Indian J Nephrol       Date:  2020-02-11

8.  Evaluation of a Two-Tier Screening Pathway for Congenital Adrenal Hyperplasia in the New South Wales Newborn Screening Programme.

Authors:  Fei Lai; Shubha Srinivasan; Veronica Wiley
Journal:  Int J Neonatal Screen       Date:  2020-08-12

9.  Non-Classical Congenital Adrenal Hyperplasia-Causing Alleles in Adolescent Girls with PCOS and in Risk Group for PCOS Development.

Authors:  Lasma Lidaka; Laine Bekere; Gunta Lazdane; Iveta Dzivite-Krisane; Anda Kivite-Urtane; Linda Gailite
Journal:  Diagnostics (Basel)       Date:  2021-05-28

10.  Polycystic Ovary Syndrome Among Female Adolescents With Congenital Adrenal Hyperplasia.

Authors:  Marwa H Abdelhamed; Waad M Al-Ghamdi; Abdulmoein E Al-Agha
Journal:  Cureus       Date:  2021-12-25
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