D016715 Proteus syndrome, also known as Wiedemann syndrome (named - TopicsExpress



          

D016715 Proteus syndrome, also known as Wiedemann syndrome (named after the German paediatrician Hans-Rudolf Wiedemann), is a congenital disorder[1]:554 that causes skin overgrowth and atypical bone development, often accompanied by tumors over half the body.[2]:776 Proteus syndrome is highly variable,[3] and is named after the Greek sea-god Proteus, who could change his shape. The condition appears to have been first described in the American medical literature by Drs. Samia Temtamy and John Rogers in 1976[4][5] Dr. Michael Cohen described it in 1979,[6] only a few more than 200 cases have been confirmed worldwide, with estimates that about 120 people are currently alive with the condition.[7] As attenuated forms of the disease may exist, there could be many people with Proteus syndrome who remain undiagnosed. Those most readily diagnosed are also the most severely disfigured Proteus syndrome causes an overgrowth of skin, bones, muscles, fatty tissues, and blood and lymphatic vessels. Proteus syndrome is a progressive condition wherein children are usually born without any obvious deformities. Tumors of skin and bone growths appear as they age. The severity and locations of these various asymmetrical growths vary greatly but typically the skull, one or more limbs, and soles of the feet will be affected. There is a risk of premature death in affected individuals due to deep vein thrombosis and pulmonary embolism caused by the vessel malformations that are associated with this disorder. Because of carrying excess weight and enlarged limbs, arthritis and muscle pain may also be symptoms — as is the case for Mandy Sellars, a woman living with a form of Proteus syndrome.[8] Further risks may occur due to the mass of extra tissue. The disorder itself does not uniformly cause learning impairments: the distribution of intelligence deficits among sufferers of Proteus syndrome appears higher than that of the general population, although this is difficult to determine with statistical significance.[9] In addition, the presence of visible deformity may have a negative effect on the social experiences of the sufferer, causing cognitive and social deficits. Afflicted individuals are at increased risk for developing certain tumors including unilateral ovarian cystadenomas, testicular tumors, meningiomas, and monomorphic adenomas of the parotid gland.[citation needed]
Posted on: Sun, 15 Sep 2013 17:39:41 +0000

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