STGD1 (medical condition): A rare genetic eye disorder that affects children and involves degeneration of the macula which is responsible for central vision which allows detailed visual function such as reading.
See also:
Stargardt disease 1:
»Introduction: Stargardt disease 1
»Symptoms of Stargardt disease 1
STGD1 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that STGD1, or a subtype of STGD1,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
STGD1: Another name for Stargardt disease 1 (or close medical condition association).
»Introduction: Stargardt disease 1
»Symptoms of Stargardt disease 1
Some of the symptoms of STGD1 incude:
See full list of 9 symptoms of STGD1 (Stargardt disease 1)
Source - NIH
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