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Results 1 - 10 of 11 for morphea OR scleroderma OR lipoatrophy
  1. Systemic scleroderma is an autoimmune disorder that affects the skin and internal organs. Autoimmune disorders occur when the immune system malfunctions and attacks ...
  2. ... associated with an increased risk of developing systemic scleroderma, which is an autoimmune disorder characterized by the ... variation contributes to the increased risk of systemic scleroderma. Researchers believe that a combination of genetic and ...
  3. ... a lack of fatty tissue under the skin (lipoatrophy), primarily in the face, arms, and chest. This ... and problems with adipocyte maturation might contribute to lipoatrophy in affected individuals. It is unclear how reduced ...
  4. ... associated with an increased risk of developing systemic scleroderma, which is an autoimmune disorder characterized by the ... variations contribute to the increased risk of systemic scleroderma. Researchers believe that a combination of genetic and ...
  5. ... a lack of fatty tissue under the skin (lipoatrophy), which is another common feature of the condition. ... JB. PIK3R1 mutations cause syndromic insulin resistance with lipoatrophy. Am J Hum Genet. 2013 Jul 11;93( ...
  6. ... Health Condition MedlinePlus Genetics provides information about Systemic scleroderma More About This Health Condition MedlinePlus Genetics provides ...
  7. ... phenomenon can be associated include systemic lupus erythematosus, scleroderma, rheumatoid arthritis, and Sjögren syndrome.Primary Raynaud phenomenon ...
  8. ... condition is occasionally found in people with systemic scleroderma, systemic lupus erythematosus, critical congenital heart disease, or ...
  9. ... of Gorlin-Chaudhry-Moss syndrome, including skull abnormalities, lipoatrophy, and short distal phalanges, but includes normal genital ...
  10. ... Dietz HC. Mutations in fibrillin-1 cause congenital scleroderma: stiff skin syndrome. Sci Transl Med. 2010 Mar ...
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