Treatment of hyperthyroidism in Down syndrome: case report and review of the literature.
This single medical case reminds behavior teams that thyroid swings are common in Down syndrome and can masquerade as new behavior issues.
01Research in Context
What this study did
Doctors wrote up one adult with Down syndrome who got radioactive iodine for hyperthyroidism.
The treatment worked too well and the person became hypothyroid.
The team wanted other doctors to know the risk.
What they found
Radioiodine fixed the over-active gland but flipped it to under-active.
The authors say the place of radioiodine in Down syndrome is still unclear.
How this fits with other research
Ghaziuddin et al. (1996) already showed hypothyroidism is common in Down syndrome.
Tenenbaum et al. (2012) later tracked 109 adults and found hypothyroidism keeps sending them to hospital.
Garwood et al. (2021) saw the same pattern in 763 Italian youths.
All three papers extend the 1999 case: thyroid problems are routine, not rare, so screen early and often.
Why it matters
You are not the endocrinologist, but you spend the most face-time with clients. Watch for low energy, weight gain, or new self-injury—these can be thyroid red flags. Prompt the family to ask for a TSH blood test. Catching the slide from hyper to hypo early keeps teaching sessions on track and avoids hospital days.
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02At a glance
03Original abstract
Thyroid disorders are common in individuals with Down syndrome (DS). Hyperthyroidism occurs much less frequently than hypothyroidism in this population, but is likely to be underestimated. We report a case of an institutionalized adult male with DS and hyperthyroidism. He was treated with radioactive iodine and, when reviewed 11 weeks later, was found to be markedly hypothyroid. We also review the literature on the three treatment options for hyperthyroidism in DS: surgery, medical treatment, and radiotherapy. We concluded that the place of radioiodine in the treatment of hyperthyroid patients with DS is yet to be defined.
Research in developmental disabilities, 1999 · doi:10.1016/s0891-4222(99)00011-6