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Churg Strauss Syndrome
Allergic Angiitis, Allergic Granulomatosis, Churg-Strauss Vasculitis, CCS, allergic granulomatosis a
Churg Strauss syndrome is a rare autoimmune disorder. Autoimmune disorders occur when a person’s own immune system attacks various parts of their body. This disorder is characterized by vasculitis (inflammation of the blood and lymph vessels), which affects many organs throughout the body. People with Churg Strauss syndrome commonly have a history of asthma, although this association is not well u...
Citrullinemia is a rare inherited disorder caused by a missing or poorly functioning enzyme, named argininosuccinate synthetase. Children affected with this disorder are unable to process protein properly, and may experience vomiting, refusal to eat, abnormal drowsiness, and coma. This disorder is called citrullinemia because one of the products that build up in the body is called citrulline. A h...
Coarctation of the aorta (CoA) is a narrowing of the largest blood vessel from the heart, the aorta, which delivers blood to the body. The narrowed blood vessel is like a bottleneck, preventing blood to efficiently get from the heart out to the body. Thus, children with this condition often have problems with their blood pressure, i.e. their blood pressure is high in the upper body, but drops in...
Cockayne syndrome (CS) is a rare disorder featuring growth deficiency, premature aging, and pigmentary retinal degeneration, as well as other findings. It is a genetic disease in which people are unable to repair DNA damage occasionally produced from rapid periods of growth or environmental exposures (e.g. exposure to UV radiation from sunlight). Without this normal DNA repair process, individu...
Coffin-Lowry Syndrome (CLS)
Coffin-Lowry syndrome (CLS) is a genetic disorder characterized by mental disabilities, low muscle tone, and differences of the head, face, and skeleton.
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