Identification and functional studies of two new dual-oxidase 2 (DUOX2) mutations in a child with congenital hypothyroidism and a eutopic normal-size thyroid gland

J Clin Endocrinol Metab. 2009 Nov;94(11):4309-14. doi: 10.1210/jc.2009-0426. Epub 2009 Sep 29.

Abstract

Context: Some cases of congenital hypothyroidism (CH) are associated with a gland of normal size.

Objective: To explore the cause of organification defect in one child with CH and a eutopic thyroid gland, genetic analyses of TPO, DUOX2, and DUOXA2 genes were performed.

Patient: One child with CH, a eutopic thyroid gland, and a partial organification defect was shown after (123)I scintigraphy and perchlorate test.

Methods: In the child with the organification defect, TPO, DUOX2, and DUOXA2 genes were analyzed. The functional activity of the DUOX2 mutants was studied after expression in eukaryotic cells.

Results: No TPO or DUOXA2 gene mutations were identified. Direct sequencing of the DUOX2 gene revealed a compound heterozygous genotype for S911L and C1052Y substitutions. S911L and C1052Y caused a partial defect in H(2)O(2) production after transient expression in HeLa cells.

Conclusions: We performed a genetic analysis in one child with CH and a eutopic thyroid gland. Two new mutations in DUOX2 gene responsible for the partial deficit in the organification process were identified.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Birth Weight
  • Cesarean Section
  • Child
  • Congenital Abnormalities / genetics
  • Dual Oxidases
  • Female
  • Humans
  • Hypothyroidism / genetics*
  • Iodine Radioisotopes
  • Jaundice / genetics
  • Middle Aged
  • Mutation*
  • NADPH Oxidases / genetics*
  • Pregnancy
  • Radionuclide Imaging
  • Reference Values
  • Thyroid Function Tests
  • Thyroid Gland / anatomy & histology*
  • Thyroid Gland / diagnostic imaging
  • Thyrotropin / blood
  • Thyroxine / blood

Substances

  • Iodine Radioisotopes
  • Thyrotropin
  • Dual Oxidases
  • NADPH Oxidases
  • DUOX2 protein, human
  • Thyroxine