Literature DB >> 576528

Five cases of absence of iodide concentrating mechanism.

K Toyoshima, Y Matsumoto, M Nishida, H Yabuuchi.   

Abstract

Five cases, 2 males and 3 females, with absence of iodide concentrating mechanism are reported. Three of the five subjects are siblings and the eldest sister has no symptom to account for the cretinism. All 5 cases have improved clinically following the administration of potassium iodide and 4 cases are still in a euthyroid state without any adverse effects during a half to more than 4 years. This study suggests that the absence of iodide concentrating mechanism might be erroneously diagnosed as athyroidal cretinism or adolescent non-toxic diffuse goitre, and may at times not show any clinical symptoms.

Entities:  

Mesh:

Substances:

Year:  1977        PMID: 576528     DOI: 10.1530/acta.0.0840527

Source DB:  PubMed          Journal:  Acta Endocrinol (Copenh)        ISSN: 0001-5598


  3 in total

1.  Molecular characterization of V59E NIS, a Na+/I- symporter mutant that causes congenital I- transport defect.

Authors:  Mia D Reed-Tsur; Antonio De la Vieja; Christopher S Ginter; Nancy Carrasco
Journal:  Endocrinology       Date:  2008-03-13       Impact factor: 4.736

2.  Congenital hypothyroidism from complete iodide transport defect: long-term evolution with iodide treatment.

Authors:  R Albero; A Cerdan; F Sanchez Franco
Journal:  Postgrad Med J       Date:  1987-12       Impact factor: 2.401

3.  An extremely high dietary iodide supply forestalls severe hypothyroidism in Na+/I- symporter (NIS) knockout mice.

Authors:  Giuseppe Ferrandino; Rachel R Kaspari; Andrea Reyna-Neyra; Nabil E Boutagy; Albert J Sinusas; Nancy Carrasco
Journal:  Sci Rep       Date:  2017-07-13       Impact factor: 4.379

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.