Literature DB >> 29405999

Congenital Hypothyroidism.

Ari J Wassner1.   

Abstract

Congenital hypothyroidism is common and can cause severe neurodevelopmental morbidity. Prompt diagnosis and treatment are critical to optimizing long-term outcomes. Universal newborn screening is an important tool for detecting congenital hypothyroidism, but awareness of its limitations, repeated screening in high-risk infants, and a high index of clinical suspicion are needed to ensure that all affected infants are appropriately identified and treated. Careful evaluation will usually reveal the etiology of congenital hypothyroidism, which may inform treatment and prognosis. Early and adequate treatment with levothyroxine results in excellent neurodevelopmental outcomes for most patients with congenital hypothyroidism.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Congenital hypothyroidism; Development; Dysgenesis; Dyshormonogenesis; Levothyroxine; Neonatal thyroid

Mesh:

Substances:

Year:  2018        PMID: 29405999     DOI: 10.1016/j.clp.2017.10.004

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


  25 in total

1.  The rs1991517 polymorphism is a genetic risk factor for congenital hypothyroidism.

Authors:  Yedukondalu Kollati; Radha Rama Devi Akella; Shaik Mohammad Naushad; Maunika Thalla; G Bhanuprakash Reddy; Vijaya R Dirisala
Journal:  3 Biotech       Date:  2020-06-01       Impact factor: 2.406

Review 2.  The Role of Astrocytes in the Development of the Cerebellum.

Authors:  Ana Paula Bergamo Araujo; Raul Carpi-Santos; Flávia Carvalho Alcantara Gomes
Journal:  Cerebellum       Date:  2019-12       Impact factor: 3.847

3.  Ultrasound findings of the thyroid gland in children and adolescents.

Authors:  Elena Moschos; Hans-Joachim Mentzel
Journal:  J Ultrasound       Date:  2022-02-09

4.  Utility of Repeat Testing for Congenital Hypothyroidism in Infants with Very Low Birth Weight.

Authors:  Susan R Rose; Christopher E Blunden; Olumide O Jarrett; Kyle Kaplan; Rheta Caravantes; Henry T Akinbi
Journal:  J Pediatr       Date:  2021-11-06       Impact factor: 4.406

5.  XB130 Plays an Essential Role in Folliculogenesis Through Mediating Interactions Between Microfilament and Microtubule Systems in Thyrocytes.

Authors:  Yingchun Wang; Yun-Yan Xiang; Junichi Sugihara; Wei-Yang Lu; Xiao-Hui Liao; Peter Arvan; Samuel Refetoff; Mingyao Liu
Journal:  Thyroid       Date:  2021-12-31       Impact factor: 6.568

6.  Primary Congenital Hypothyroidism in Children Below 3 Years Old - Etiology and Treatment With Overtreatment and Undertreatment Risks, a 5-Year Single Centre Experience.

Authors:  Elżbieta Lipska; Agnieszka Lecka-Ambroziak; Daniel Witkowski; Katarzyna Szamotulska; Ewa Mierzejewska; Mariusz Ołtarzewski
Journal:  Front Endocrinol (Lausanne)       Date:  2022-06-27       Impact factor: 6.055

7.  Thyroid Deficiency Before Birth Alters the Adipose Transcriptome to Promote Overgrowth of White Adipose Tissue and Impair Thermogenic Capacity.

Authors:  Shelley E Harris; Miles J De Blasio; Xiaohui Zhao; Marcella Ma; Katie Davies; F B Peter Wooding; Russell S Hamilton; Dominique Blache; David Meredith; Andrew J Murray; Abigail L Fowden; Alison J Forhead
Journal:  Thyroid       Date:  2020-03-18       Impact factor: 6.568

8.  XB130 Deficiency Causes Congenital Hypothyroidism in Mice due to Disorganized Apical Membrane Structure and Function of Thyrocytes.

Authors:  Yingchun Wang; Hiroki Shimizu; Yun-Yan Xiang; Junichi Sugihara; Wei-Yang Lu; Xiao-Hui Liao; Hae-Ra Cho; Hiroaki Toba; Xiao-Hui Bai; Sylvia L Asa; Peter Arvan; Samuel Refetoff; Mingyao Liu
Journal:  Thyroid       Date:  2021-11       Impact factor: 6.568

9.  Identification and analyzes of DUOX2 mutations in two familial congenital hypothyroidism cases.

Authors:  Liangshan Li; Wenmiao Liu; Liqin Zhang; Fang Wang; Fengqi Wang; Maosheng Gu; Xiuli Wang; Shiguo Liu
Journal:  Endocrine       Date:  2020-08-15       Impact factor: 3.633

10.  Neonatal Dyshormonogenetic Goiter with Hypothyroidism Associated with Novel Mutations in Thyroglobulin and SLC26A4 Gene.

Authors:  Valeria Calcaterra; Rossella Lamberti; Claudia Viggiano; Sara Gatto; Luigina Spaccini; Gianluca Lista; Gianvincenzo Zuccotti
Journal:  Pediatr Rep       Date:  2021-05-02
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