Artículo

Variable clinical presentation and outcome in pediatric patients with resistance to thyroid hormone (RTH)

Chiesa, Ana Elena Icon; Olcese, María Cecilia ; Papendieck, Patricia ; Martinez, Alicia Susana Icon; Vieites, Ana María ; Bengolea, Sonia ; Targovnik, Hector Manuel Icon; Rivolta, Carina Marcela Icon; Gruñeiro Papendieck, Laura

Otros responsables

Fecha

02/2012

Editorial

Springer

Revista

Endocrine

Título del libro

Nombre del evento

Fecha del evento

Institución organizadora

ISSN

0969-711X

eISSN

1559-0100

ISBN

Idioma

Inglés

Tipo del evento

Clasificación temática

Resumen

Resistance to thyroid hormone (RTH) is characterized by elevated levels of thyroid hormones, normal or slightly increased TSH levels respondent to TRH, resistance to thyroid hormone administration, and variable clinical expression. To describe the diverse clinical and biochemical findings of six children from five unrelated families with molecular diagnosis of RTH (0.5–12.7 years) and their follow-up (3–20 years). All RTH patients and 4 affected parents’ harbored mutations in exons 9 or 10 of the thyroid receptor β gene: p.M313T (de novo), pN331D, p.L341P, p.L346F, and p.P453L. At consultation 5/6 had goiter, 4/6 tachycardia, and 3/5 learning disabilities. Median hormone levels were: T4 257.4 nmol/l (NR: 77.2–180.2); FreeT4 39.9 pmol/(NR:10.3–28.3); T3 4.28 nmol/l (NR:1.23–3.39) TSH 2.8 mUI/l (NR: 0.5–5) always responsive to TRH. TSH levels remained detectable after supraphysiologic T3 administration while SHBG levels showed a paradoxical decrease in 4/6. Thyroid antibodies, initially present in two subjects, became positive in other two during follow-up. All patients grew normally and presented variable symptoms that were treated according to need. Two patients developed psychiatric disorders. Only one of the four affected parents exhibited clinical signs of RTH (tachycardia and depression). Parent’s thyroid profile showed similar TSH and T3 levels but lower T4 and FT4 than their children. RTH has a distinctive biochemical profile with highly variable clinical manifestations and outcomes. Its recognition and molecular characterization avoid misleading diagnosis. Treatment has to be instituted according to each subject’s own clinical requirements.

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