Molecular pathogenesis of neonatal hypothyroidism

Horm Res. 2000:53 Suppl 1:12-8. doi: 10.1159/000053199.

Abstract

In patients with congenital hypothyroidism (CH), the autosomal recessive inheritance of mutations of thyroid peroxidase, thyroglobulin and the NIS and pendrin genes encoding for sodium iodide transporters has been identified. CH due to thyroid dysgenesis was considered to be a sporadic disease, but recently, inheritable defects of thyroid development have been described. The autosomal recessive inheritance of mutations of the thyroid-stimulating hormone receptor gene was recognized in patients with CH and thyroid hypoplasia, while autosomal dominant mutations of the Pax-8 gene were described in patients with thyroid dysgenesis. In addition, analysis of mutations of the beta-thyrotropin gene has resulted in a new understanding of the pathogenesis of central CH. Molecular genetic studies in patients with CH detected by newborn screening will provide the information necessary for genetic counselling and may help to explain the less favourable outcome present in 5-10% of the patients.

Publication types

  • Review

MeSH terms

  • Carrier Proteins / genetics
  • Congenital Hypothyroidism
  • Humans
  • Hypothyroidism / genetics*
  • Infant, Newborn
  • Iodide Peroxidase / genetics
  • Membrane Proteins / genetics
  • Membrane Transport Proteins*
  • Mutation*
  • Receptors, Thyrotropin / genetics
  • Sulfate Transporters
  • Symporters*
  • Thyroglobulin / genetics
  • Thyrotropin / genetics
  • Transcription Factors / genetics

Substances

  • Carrier Proteins
  • Membrane Proteins
  • Membrane Transport Proteins
  • Receptors, Thyrotropin
  • SLC26A4 protein, human
  • Sulfate Transporters
  • Symporters
  • Transcription Factors
  • sodium-iodide symporter
  • Thyrotropin
  • Thyroglobulin
  • Iodide Peroxidase