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Differential Diagnosis For Cherry red spot/retinal sign

List of current finding(s):

Cherry red spot/retinal sign
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Metabolic, Storage Disorders: Mucopolysaccharidoses; Hurler's mucopolysaccharidosis syndrome; Tay-Sachs disease; Cerebral Gaucher's of infants (acute); Sialidosis/Cherry Red Spot Myoclonus; Beta-glucuronidase deficiency syndrome (MPS VII); Farber disease/ceramide lipidosis; Gangliosidosis, generalized (GM1); Juvenile ceroid lipofuscinosis/Batten-M; Niemann-Pick disease; Sandhoff disease; Goldberg Syndrome; Lysosome Storage Disease
Congenital, Developmental Disorders: Amaurosis, congenital, Leber
Hereditary, Familial, Genetic Disorders: Hallervorden-Spatz disease (PKAN/NBIA); Leukodystrophy, Krabbe
Usage, Degenerative, Necrosis, Age Related Disorders: Metachromatic leukodystrophy
Arteriosclerotic, Vascular, Venous Disorders: Retinal Artery Occlusion/Thrombosis
Drugs: Quinine Administration/Toxicity; Dapsone (avlosulfone) Administration/Toxicity
Poisoning (Specific Agent): Carbon monoxide poisoning/exposure; Methanol ingestion/poisoning
Definition: Be the first to add a definition for Cherry red spot/retinal sign
External Links Related to Cherry red spot/retinal sign: Google; Wikipedia; Merck; Images; PubMed (National Library of Medicine); NGC (National Guideline Clearinghouse); Medscape (eMedicine); Harrison's Online (accessmedicine); NEJM (The New England Journal of Medicine)

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