PKDTS (medical condition): A rare genetic disorder characterized by numerous kidney cysts and hamartomas (benign nodules that can occur in the skin or various organs including the brain).
See also:
Polycystic kidneys, severe infantile, with tuberous sclerosis:
»Introduction: Polycystic kidneys, severe infantile, with tuberous sclerosis
»Symptoms of Polycystic kidneys, severe infantile, with tuberous sclerosis
PKDTS is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that PKDTS, or a subtype of PKDTS,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
PKDTS: Another name for Polycystic kidneys, severe infantile, with tuberous sclerosis (or close medical condition association).
»Introduction: Polycystic kidneys, severe infantile, with tuberous sclerosis
»Symptoms of Polycystic kidneys, severe infantile, with tuberous sclerosis
Some of the symptoms of PKDTS incude:
Read more about symptoms of PKDTS (Polycystic kidneys, severe infantile, with tuberous sclerosis)
Source - NIH
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