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Graves' ophthalmopathy, also known as thyroid eye disease ( TED ), is an autoimmune inflammatory disorder of the orbit and periorbital tissues, characterized by upper eyelid retraction, lid lag, swelling, redness ( erythema ), conjunctivitis, and bulging eyes ( exophthalmos ). [ 1] It occurs most commonly in individuals with Graves' disease ...
Graves disease, also known as toxic diffuse goiter or Basedow’s disease, is an autoimmune disease that affects the thyroid. [ 1] It frequently results in and is the most common cause of hyperthyroidism. [ 5] It also often results in an enlarged thyroid. [ 1] Signs and symptoms of hyperthyroidism may include irritability, muscle weakness ...
Stargardt disease is the most common inherited single-gene retinal disease. [ 1] In terms of the first description of the disease, [ 2] it follows an autosomal recessive inheritance pattern, which has been later linked to bi-allelic ABCA4 gene variants (STGD1).
Plus, seeing a specialist can mean that you get the diagnosis and treatment that you need more quickly. That time may help you stave off long-term damage that can be caused by the disease, he adds.
Chronic progressive external ophthalmoplegia ( CPEO) is a type of eye disorder characterized by slowly progressive inability to move the eyes and eyebrows. [ 1] It is often the only feature of mitochondrial disease, in which case the term CPEO may be given as the diagnosis. In other people suffering from mitochondrial disease, CPEO occurs as ...
Graves’ disease is an autoimmune condition that causes excess thyroid hormone. Symptoms can include rapid heartbeat, weight loss, and protruding eyes. It might be caused by a genetic ...
Myasthenia gravis ( MG) is a long-term neuromuscular junction disease that leads to varying degrees of skeletal muscle weakness. [ 1] The most commonly affected muscles are those of the eyes, face, and swallowing. [ 1][ 5] It can result in double vision, drooping eyelids, and difficulties in talking and walking. [ 1]
Ocular myasthenia. Ocular myasthenia gravis (MG) is a disease of the neuromuscular junction resulting in hallmark variability in muscle weakness and fatigability. MG is an autoimmune disease where anomalous antibodies are produced against the naturally occurring acetylcholine receptors in voluntary muscles. MG may be limited to the muscles of ...