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Resistance to thyrotropin: familial case report

Two female dizygotic twins with subclinical primary hypothyroidism due to homozygous p.R450H mutation in TSHR gene are presented. A 5-year follow-up in both cases showed no progression of thyroid dysfunction. Indications for levothyroxine replacement in subclinical hypothyroidism are discussed.

Uloženo v:
Hlavní autoři: Mariya Aleksandrovna Osipovskaya, Alexey Vasil'evich Kiyaev, Nina Alekseevna Makretskaya, Evgeny Viktorovich Vasiliev, Anatoly Nikolaevich Tiulpakov
Médium: Artigo
Jazyk:Russo
Vydáno: Endocrinology Research Centre 2016-02-01
Edice:Клиническая и экспериментальная тиреоидология
Témata:
subclinical hypothyroidism
resistance to thyrotropin
tshr
children
On-line přístup:https://cet-endojournals.ru/ket/article/viewFile/7699/5652
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