Ostravik lindemann solberg syndrome (medical condition): A very rare syndrome characterized mainly by webbed fingers, congenital heart defects and tongue tumors.
See also:
Heart defect, tongue hamartoma and polysyndactyly:
»Introduction: Heart defect, tongue hamartoma and polysyndactyly
»Symptoms of Heart defect, tongue hamartoma and polysyndactyly
Ostravik lindemann solberg syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Ostravik lindemann solberg syndrome, or a subtype of Ostravik lindemann solberg 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 if affects 1 person per 2,000.
They list Ostravik lindemann solberg syndrome as a "rare disease".
Source - Orphanet
Ostravik lindemann solberg syndrome: Another name for Heart defect, tongue hamartoma and polysyndactyly (or close medical condition association).
»Introduction: Heart defect, tongue hamartoma and polysyndactyly
»Symptoms of Heart defect, tongue hamartoma and polysyndactyly
Some of the symptoms of Ostravik lindemann solberg syndrome incude:
Source - NIH
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