Literature DB >> 15817507

Molecular basis of adrenal insufficiency.

Kenji Fujieda1, Toshihiro Tajima.   

Abstract

Defective production of adrenal steroids due to either primary adrenal failure or hypothalamic-pituitary impairment of the corticotrophic axis causes adrenal insufficiency. Depending on the etiologies of adrenal insufficiency, clinical manifestations may be severe or mild, have gradual or sudden onset, begin in infancy or childhood/adolescence. Adrenal crisis represents an endocrine emergency, and thus the rapid recognition and prompt therapy for adrenal crisis are critical for survival even before the diagnosis is made. The recognition of various disorders that cause adrenal insufficiency, either at a clinical or molecular level, often has implications for the management of the patient. Recent molecular-genetic analysis for the disorder that causes adrenal insufficiency gives valuable insights into the adrenal organogenesis, the regulation of steroid hormone biosynthesis, and the developmental and reproductive endocrinology. In this review we present the latest information on the molecular basis of adrenal insufficiency, with special emphasis on congenital lipoid adrenal hyperplasia, P450-oxidoreductase deficiency, and adrenal hypoplasia congenita.

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Year:  2005        PMID: 15817507     DOI: 10.1203/01.PDR.0000159568.31749.4D

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  8 in total

1.  The genetic basis of adrenal gland weight and structure in BXD recombinant inbred mice.

Authors:  Domenico L Di Curzio; Daniel Goldowitz
Journal:  Mamm Genome       Date:  2011-02-24       Impact factor: 2.957

2.  Clinical guidelines for the diagnosis and treatment of 21-hydroxylase deficiency (2021 revision).

Authors:  Tomohiro Ishii; Kenichi Kashimada; Naoko Amano; Kei Takasawa; Akari Nakamura-Utsunomiya; Shuichi Yatsuga; Tokuo Mukai; Shinobu Ida; Mitsuhisa Isobe; Masaru Fukushi; Hiroyuki Satoh; Kaoru Yoshino; Michio Otsuki; Takuyuki Katabami; Toshihiro Tajima
Journal:  Clin Pediatr Endocrinol       Date:  2022-04-10

Review 3.  Biomarkers, metabonomics, and drug development: can inborn errors of metabolism help in understanding drug toxicity?

Authors:  Subrahmanyam Vangala; Alfred Tonelli
Journal:  AAPS J       Date:  2007-07-20       Impact factor: 4.009

4.  Severe loss-of-function mutations in the adrenocorticotropin receptor (ACTHR, MC2R) can be found in patients diagnosed with salt-losing adrenal hypoplasia.

Authors:  Lin Lin; Peter C Hindmarsh; Louise A Metherell; Mahmoud Alzyoud; Maryam Al-Ali; Caroline E Brain; Adrian J L Clark; Mehul T Dattani; John C Achermann
Journal:  Clin Endocrinol (Oxf)       Date:  2007-02       Impact factor: 3.478

5.  Non-conventional Genetic Basis of Congenital Adrenal Hypoplasia in South Asia.

Authors:  Sudip Chatterjee; Anirban Majumder
Journal:  Cureus       Date:  2022-03-26

6.  Skewed X inactivation is associated with phenotype in a female with adrenal hypoplasia congenita.

Authors:  M G Shaikh; L Boyes; H Kingston; R Collins; G T N Besley; B Padmakumar; O Ismayl; I Hughes; C M Hall; C Hellerud; J C Achermann; P E Clayton
Journal:  J Med Genet       Date:  2008-09       Impact factor: 6.318

7.  Clinical features of congenital adrenal insufficiency including growth patterns and significance of ACTH stimulation test.

Authors:  Ji Won Koh; Gu Hwan Kim; Han Wook Yoo; Jeesuk Yu
Journal:  J Korean Med Sci       Date:  2013-10-31       Impact factor: 2.153

Review 8.  The Insulin/IGF System in Mammalian Sexual Development and Reproduction.

Authors:  Yasmine Neirijnck; Marilena D Papaioannou; Serge Nef
Journal:  Int J Mol Sci       Date:  2019-09-09       Impact factor: 5.923

  8 in total

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