Genetics of congenital hypothyroidism: Modern concepts. Issue 2 (14th May 2022)
- Record Type:
- Journal Article
- Title:
- Genetics of congenital hypothyroidism: Modern concepts. Issue 2 (14th May 2022)
- Main Title:
- Genetics of congenital hypothyroidism: Modern concepts
- Authors:
- Stoupa, Athanasia
Kariyawasam, Dulanjalee
Polak, Michel
Carré, Aurore - Abstract:
- ABSTRACT: Congenital hypothyroidism (CH) is the most common neonatal endocrine disorder and one of the most common preventable causes of intellectual disability in the world. CH may be due to developmental or functional thyroid defects (primary or peripheral CH) or be hypothalamic‐pituitary in origin (central CH). In most cases, primary CH is caused by a developmental malformation of the gland (thyroid dysgenesis, TD) or by a defect in thyroid hormones synthesis (dyshormonogenesis, DH). TD represents about 65% of CH and a genetic cause is currently identified in fewer than 5% of patients. The remaining 35% are cases of DH and are explained with certainty at the molecular level in more than 50% of cases. The etiology of CH is mostly unknown and may include contributions from individual and environmental factors. In recent years, the detailed phenotypic description of patients, high‐throughput sequencing technologies, and the use of animal models have made it possible to discover new genes involved in the development or function of the thyroid gland. This paper reviews all the genetic causes of CH. The modes by which CH is transmitted will also be discussed, including a new oligogenic model. CH is no longer simply a dominant disease for cases of CH due to TD and recessive for cases of CH due to DH, but a far more complex disorder. Abstract : Proposed model of congenital hypothyroidism: complex and multi‐factor pathology. Dark blue: scientifically proven factor; light blue:ABSTRACT: Congenital hypothyroidism (CH) is the most common neonatal endocrine disorder and one of the most common preventable causes of intellectual disability in the world. CH may be due to developmental or functional thyroid defects (primary or peripheral CH) or be hypothalamic‐pituitary in origin (central CH). In most cases, primary CH is caused by a developmental malformation of the gland (thyroid dysgenesis, TD) or by a defect in thyroid hormones synthesis (dyshormonogenesis, DH). TD represents about 65% of CH and a genetic cause is currently identified in fewer than 5% of patients. The remaining 35% are cases of DH and are explained with certainty at the molecular level in more than 50% of cases. The etiology of CH is mostly unknown and may include contributions from individual and environmental factors. In recent years, the detailed phenotypic description of patients, high‐throughput sequencing technologies, and the use of animal models have made it possible to discover new genes involved in the development or function of the thyroid gland. This paper reviews all the genetic causes of CH. The modes by which CH is transmitted will also be discussed, including a new oligogenic model. CH is no longer simply a dominant disease for cases of CH due to TD and recessive for cases of CH due to DH, but a far more complex disorder. Abstract : Proposed model of congenital hypothyroidism: complex and multi‐factor pathology. Dark blue: scientifically proven factor; light blue: factor as yet unproven or unclear. … (more)
- Is Part Of:
- Pediatric investigation. Volume 6:Issue 2(2022)
- Journal:
- Pediatric investigation
- Issue:
- Volume 6:Issue 2(2022)
- Issue Display:
- Volume 6, Issue 2 (2022)
- Year:
- 2022
- Volume:
- 6
- Issue:
- 2
- Issue Sort Value:
- 2022-0006-0002-0000
- Page Start:
- 123
- Page End:
- 134
- Publication Date:
- 2022-05-14
- Subjects:
- Congenital hypothyroidism -- Development -- Genetic -- High‐throughput sequencing -- Thyroid dysgenesis -- Dyshormonogenesis -- Oligogenism
Pediatrics -- Periodicals
Pediatrics -- Research -- Periodicals
618.920005 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2574-2272 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/ped4.12324 ↗
- Languages:
- English
- ISSNs:
- 2574-2272
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 22132.xml