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โ† Trials
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The Natural History of Familial Dysautonomia

Recruitingn/aAges 4 Years - anyAllNYU Langone Health
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In plain words

What the trial is, and whether it could suit you

The study will collect clinical information from patients with FD and allow them to give blood to help develop biological markers of the disease to aid diagnosis and treatment. This is a non-invasive, non-interventional, observation study that poses only minimal risk for participants. The study will document the clinical features of patients with FD overtime by storing their routine clinical test results in a central database. The study will involve collaborators at other specialist clinics around the world who follow/evaluate patients with FD annually. Providing blood for future use is optional.

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: * Patients of any age with a diagnosis of familial dysautonomia (FD) with molecular confirmation of the IKBKAP mutation. * Ability to provide informed consent (or assent) and comply with the study protocol Exclusion Criteria: * Subjects that do not wish to be a part of the study.
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What it tests

  • Not listed
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Where

2 sites
Dysautonomia Center - School of Medicine -NYU Langone Medical Center
New York, United States
Sheba Medical Center - Safra Children's Hospital
Tel Litwinsky, Israel
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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