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Osteoporosis-pseudoglioma syndrome (medical condition): A rare genetic disorder characterized by early onset of osteoporosis (during childhood) and loss of vision resulting from retinal detachment due to a retinal pseudoglioma (inflammatory eye condition).
See also:
Osteoporosis-pseudoglioma syndrome:
»Introduction: Osteoporosis-pseudoglioma syndrome
»Symptoms of Osteoporosis-pseudoglioma syndrome
Osteoporosis-pseudoglioma syndrome: A rare syndrome characterized by generalized osteoporosis, pseudoglioma, and blindness usually due to retinal detachment. Mental retardation and ligamental laxity are variable manifestations.
Source: Diseases Database
These medical condition or symptom topics may be relevant to medical information for Osteoporosis-pseudoglioma syndrome:
Osteoporosis-pseudoglioma syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Osteoporosis-pseudoglioma syndrome, or a subtype of Osteoporosis-pseudoglioma 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 Osteoporosis-pseudoglioma syndrome as a "rare disease".
Source - Orphanet
Osteoporosis-pseudoglioma syndrome (medical condition): See Osteoporosis-pseudoglioma syndrome (disease information).
»Introduction: Osteoporosis-pseudoglioma syndrome
»Symptoms of Osteoporosis-pseudoglioma syndrome
Source - NIH
Source: Diseases Database
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