Literature DB >> 29406008

Congenital Hypopituitarism.

John S Parks1.   

Abstract

Mutations of growth hormone genes and pituitary transcription factors account for a small proportion of cases of severe congenital hypopituitarism. Most cases show characteristic MRI findings of pituitary stalk interruption syndrome. Clinical suspicion should prompt assessment of cortisol, free T4, thyroid-stimulating hormone, and growth hormone levels together with MRI of the hypothalamic and pituitary regions.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cholestasis; Growth hormone; Guidelines; Hypoglycemia; Hypopituitarism; MRI; Pituitary stalk

Mesh：

Substances：

Year:  2018        PMID： 29406008     DOI： 10.1016/j.clp.2017.11.001

Source DB:  PubMed          Journal:  Clin Perinatol        ISSN： 0095-5108            Impact factor:   3.430


  10 in total

Review 1.  Hypopituitarism Related Cholestatic Jaundice: Important to Recognise, Rewarding to Treat but Difficult to Diagnose!

Authors:  Rishi Bolia; Anshu Srivastava
Journal:  Indian J Pediatr       Date:  2019-03-13       Impact factor: 1.967

2.  Expert consensus on the clinical practice of neonatal brain magnetic resonance imaging.

Authors: 
Journal:  Zhongguo Dang Dai Er Ke Za Zhi       Date:  2022-01-15

Review 3.  Advances in differential diagnosis and management of growth hormone deficiency in children.

Authors:  Camille Hage; Hoong-Wei Gan; Anastasia Ibba; Giuseppa Patti; Mehul Dattani; Sandro Loche; Mohamad Maghnie; Roberto Salvatori
Journal:  Nat Rev Endocrinol       Date:  2021-08-20       Impact factor: 43.330

4.  Risk of Mental Illnesses in Patients With Hypopituitarism: A Nationwide Population-Based Cohort Study.

Authors:  I-Hua Wei; Chih-Chia Huang
Journal:  Psychiatry Investig       Date:  2022-06-15       Impact factor: 3.202

5.  Hypoglycemia and jaundice in newborns with pituitary stalk interruption syndrome.

Authors:  Qi Wang; Xiangji Meng; Yan Sun; Fan Liu; Chao Xu; Yu Qiao; Jianmei Yang; Guimei Li; Yulin Wang
Journal:  Medicine (Baltimore)       Date:  2021-05-14       Impact factor: 1.889

Review 6.  Congenital Hypopituitarism During the Neonatal Period: Epidemiology, Pathogenesis, Therapeutic Options, and Outcome.

Authors:  Laura Bosch I Ara; Harshini Katugampola; Mehul T Dattani
Journal:  Front Pediatr       Date:  2021-02-02       Impact factor: 3.418

7.  Congenital hypopituitarism in two brothers with a duplication of the 'acrogigantism gene' GPR101: clinical findings and review of the literature.

Authors:  Melitza S M Elizabeth; Annemieke J M H Verkerk; Anita C S Hokken-Koelega; Joost A M Verlouw; Jesús Argente; Roland Pfaeffle; Sebastian J C M M Neggers; Jenny A Visser; Laura C G de Graaff
Journal:  Pituitary       Date:  2020-11-13       Impact factor: 4.107

8.  Case Report: A Detailed Phenotypic Description of Patients and Relatives with Combined Central Hypothyroidism and Growth Hormone Deficiency Carrying IGSF1 Mutations.

Authors:  Melitza S M Elizabeth; Anita Hokken-Koelega; Jenny A Visser; Sjoerd D Joustra; Laura C G de Graaff
Journal:  Genes (Basel)       Date:  2022-03-30       Impact factor: 4.141

Review 9.  Delayed Diagnosis of Congenital Combined Pituitary Hormone Deficiency including Severe Growth Hormone Deficiency in Children with Persistent Neonatal Hypoglycemia-Case Reports and Review.

Authors:  Joanna Smyczyńska; Natalia Pawelak; Maciej Hilczer; Andrzej Lewiński
Journal:  Int J Mol Sci       Date:  2022-09-21       Impact factor: 6.208

Review 10.  Growth hormone deficiency and replacement in children.

Authors:  Margaret C S Boguszewski
Journal:  Rev Endocr Metab Disord       Date:  2020-10-08       Impact factor: 6.514
  10 in total

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