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Progressive cataract
- About Progeria (National Human Genome Research Institute)Progeria is an extremely rare genetic disease of childhood characterized by dramatic, premature aging. ... Genetic Disorders/Specifics ... Genetic Disorders ... National ...
- Usher Syndrome (Genetic and Rare Diseases Information Center)Usher Syndrome/Learn More ... Usher Syndrome ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Find symptoms and other information ...
- Hereditary Spastic Paraplegia (National Institute of Neurological Disorders and Stroke)Leg Injuries and Disorders/Specifics ... Leg Injuries and Disorders ... Paralysis/Specifics ... Paralysis ... Neuromuscular Disorders/Specifics ... Neuromuscular Disorders ... Peripheral ...
- Usher Syndrome (National Institute on Deafness and Other Communication Disorders)Usher Syndrome/Learn More ... Usher Syndrome ... National Institute on Deafness and Other Communication Disorders ... From the National Institutes of Health ... Usher syndrome ...
- Muscular Dystrophy (National Institute of Neurological Disorders and Stroke)... to a group of genetic diseases that cause progressive weakness and degeneration of skeletal muscles. These disorders ( ...
- Learning about Marfan Syndrome (National Human Genome Research Institute)Marfan Syndrome/Start Here ... Marfan Syndrome ... National Human Genome Research Institute ... From the National Institutes of Health ... Marfan syndrome an inherited disorder ...
- About Myotonic Dystrophy (National Human Genome Research Institute)Muscular Dystrophy/Genetics ... Muscular Dystrophy ... National Human Genome Research Institute ... From the National Institutes of Health ... Myotonic dystrophy is an inherited ...
- Behcet Disease (Genetic and Rare Diseases Information Center)Behcet's Syndrome/Learn More ... Behcet's Syndrome ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Find symptoms and other ...