Thyroid dyshormonogenesis 2A
MONDO:0010133Thyroid peroxidase system defect due to presumed mutation(s) in the TPO gene, resulting in decreased activity of thyroid peroxidase.
Also known as: TDH2A, TPO familial thyroid dyshormonogenesis, familial thyroid dyshormonogenesis caused by mutation in TPO, hypothyroidism, congenital, due to dyshormonogenesis, 2A, thyroid dyshormonogenesis 2A, thyroid dyshormonogenesis type 2A, thyroid hormonogenesis, genetic defect in, 2A, iodide peroxidase deficiency
5 clinical trials for this condition and its sub-types, 4 tagged with Thyroid dyshormonogenesis 2A itself.
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Stem cell hope for rare brain disease: new expanded access trial opens
Disease control Expanded accessThis study offers expanded access to an experimental stem cell treatment for up to 7 adults with Multiple System Atrophy (MSA), a rare and serious brain disorder. Participants will receive 12 intravenous infusions and 6 spinal injections of donor stem cells over 44 weeks. The goa…
Sponsor: Hope Biosciences Research Foundation • Aim: Disease control
Last updated Jun 27, 2026 12:09 UTC
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New protein therapy hopes to repair brain damage in rare disease
Disease control Recruiting nowThis early-phase trial tests a drug called Aleeto, a nerve repair protein made from stem cells, in 20 people with Multiple System Atrophy (MSA), a rare brain disease. The study checks if Aleeto is safe and might help with symptoms. Participants receive the drug via injection into…
Early phase 1 • Sponsor: Beijing Tiantan Hospital • Aim: Disease control
Last updated Jun 26, 2026 12:56 UTC
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Blood test breakthrough could spot Parkinson's before symptoms worsen
Diagnosis Recruiting nowThis study is testing a new blood test to help doctors diagnose Parkinson's disease and similar brain disorders more accurately and earlier. Researchers will use a technique called RT-QuIC to detect misfolded proteins in blood samples from 458 participants, including healthy peop…
Sponsor: Xuanwu Hospital, Beijing • Aim: Diagnosis
Last updated Jun 27, 2026 12:01 UTC