Oculocerebrorenal Dystrophy (Lowe Syndrome): eMedicine Pediatrics: Genetics and Metabolic Disease
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Oculocerebrorenal Dystrophy (Lowe Syndrome): eMedicine Pediatrics: Genetics and Metabolic Disease
Overview: In 1952, Lowe and colleagues described an infant with congenital cataracts and mental retardation. When more patients were described, the phenotype was expanded to include the renal tubular defects that comprise Fanconi syndrome, and an X-linked ...
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Tags: Genetic, Metabolic, Disease and Condition, Healthy Living, Children's Health, disease, Medical, Genetics
Most Recently Shared on July 15, 2009 at 7:45 pm By:
The Lowe Syndrome eMedicine topic has been updated with new information for 2009. http://bit.ly/bWZqq #pediatrics #health #medicine
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