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Wagner syndrome: a genetic condition caused by a mutation in the gene (CSPG2 on chromosome 5) encoding chondroitin sulfate proteoglycan-2, also known as versican. Versican is a substance present in the vitreous body of the eye. Symptoms and signs include changes in the vitreous body of the eye, retinal detachment, cataracts, and poor visual adaptation to dark. An association with cleft palate has been described. Studies suggest an irregular autosomal dominant pattern of inheritance.
wagner. everything about Wagner disease: symptoms and genetics, treat-ments, usual and otherwise, stem cell and gene therapie
Wagner syndrome is a hereditary disorder that causes progressive vision loss. Loss of vision usually begins in adulthood, although some individuals are ...
Featured Image. Picture of Psoriasis. A reddish, scaly rash often located over the surfaces of the elbows, knees, scalp, and around or in the ears, navel, genitals or buttocks...
Wagner's disease is a very rare hereditary eye disorder. Lesions develop on the connective tissue of the eye, and the patient can become blind. Children born to ...
Wagner syndrome is a rare hereditary vitreo-retinal disease. It is one of the connective tissue disorders affecting the collagen. The main feature is an ‘empty ...