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Opitz syndrome: A rare genetic disorder characterized by wide-set eyes, hypospadias and swallowing difficulties. More detailed information about the symptoms, causes, and treatments of Opitz syndrome is available below.
See full list of 18 symptoms of Opitz syndrome
Read more about causes of Opitz syndrome.
Research the causes of these diseases that are similar to, or related to, Opitz syndrome:
See full list of 31 occasional symptoms of Opitz syndrome
Medical research articles related to Opitz syndrome include:
Click here to find more evidence-based articles on the TRIP Database
Visit our research pages for current research about Opitz syndrome treatments.
The US based website ClinicalTrials.gov lists information on both federally and privately supported clinical trials using human volunteers.
Some of the clinical trials listed on ClinicalTrials.gov for Opitz syndrome include:
See full list of 8 Clinical Trials for Opitz syndrome
Types of Opitz syndrome
Read about other experiences, ask a question about Opitz syndrome, or answer someone else's question, on our message boards:
Opitz syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Opitz syndrome, or a subtype of Opitz syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Opitz syndrome as a "rare disease".
Source - Orphanet
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