Rapadilino syndrome
Rapadilino syndrome: Introduction
Rapadilino syndrome: A rare genetic condition characterized primarily by a cleft palate which has a high arch and missing or underdeveloped kneecaps as well as other anomalies.
More detailed information about the symptoms,
causes, and treatments of Rapadilino syndrome is available below.
Symptoms of Rapadilino syndrome
See full list of 10
symptoms of Rapadilino syndrome
Wrongly Diagnosed with Rapadilino syndrome?
Rapadilino syndrome: Related Patient Stories
Causes of Rapadilino syndrome
Read more about causes of Rapadilino syndrome.
More information about causes of Rapadilino syndrome:
Disease Topics Related To Rapadilino syndrome
Research the causes of these diseases that are similar to, or related to, Rapadilino syndrome:
Misdiagnosis and Rapadilino syndrome
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Read more about Misdiagnosis and Rapadilino syndrome
Rapadilino syndrome: Research Doctors & Specialists
Research related physicians and medical specialists:
- Bone, Joint and Orthopedic Specialists:
- Ear, Nose & Throat Specialists:
- Arthritis & Joint Health Specialists (Rheumatology):
- more specialists...»
Other doctor, physician and specialist research services:
Evidence Based Medicine Research for Rapadilino syndrome
Medical research articles related to Rapadilino syndrome include:
Click here to find more evidence-based articles on the TRIP Database
Rapadilino syndrome: Animations
More Rapadilino syndrome animations & videos
Research about Rapadilino syndrome
Visit our research pages for current research about Rapadilino syndrome treatments.
Statistics for Rapadilino syndrome
Rapadilino syndrome: Broader Related Topics
Types of Rapadilino syndrome
User Interactive Forums
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Definitions of Rapadilino syndrome:
Rapadilino syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Rapadilino syndrome, or a subtype of Rapadilino 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 Rapadilino syndrome as a "rare disease".
Source - Orphanet
Contents for Rapadilino syndrome: