The Clinical Spectrum of Resistance to Thyroid Hormone Alpha in Children and Adults

被引:14
作者
Erbas, Ibrahim Mert [1 ]
Demir, Korcan [1 ]
机构
[1] Dokuz Eylul Univ, Dept Pediat Endocrinol, Fac Med, Izmir, Turkey
关键词
Constipation; developmental delay; growth failure; central hypothyroidism; autism spectrum disorder; LT4; impaired sensitivity to thyroid hormone; LIGAND-BINDING DOMAIN; POSTNATAL-DEVELOPMENT; FOLLOW-UP; RECEPTOR; MUTATION; MICE; TRANSPORTER; THYROID-HORMONE-RECEPTOR-ALPHA-1; PSYCHOMOTOR; PHENOTYPE;
D O I
10.4274/jcrpe.galenos.2020.2019.0190
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Resistance to thyroid hormone alpha occurs due to pathogenic, heterozygous variants in THRA. The entity was first described in 2012 and to date only a small number of patients with varying severity have been reported. In this review, we summarize and interpret the heterogeneous clinical and laboratory features of all published cases, including ours. Many symptoms and findings are similar to those seen in primary hypothyroidism. However, thyroid-stimulating hormone levels are normal. Free triiodothyronine (T3) levels are in the upper half of normal range or frankly high and free thyroxine (T4) levels are low or in the lower half of normal range. Alterations in free T3 and free T4 may not be remarkable, particularly in adults, possibly contributing to underdiagnosis. In such patients, low reverse T3 levels, normo- or macrocytic anemia or, particularly in children, mildly elevated creatine kinase levels would warrant THRA sequencing. Treatment with L-thyroxine results in improvement of some clinical findings.
引用
收藏
页码:1 / 14
页数:14
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