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Results 1 - 7 of 7 for morphea OR lipoatrophy OR scleroderma
  1. STAT4 gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/stat4 - Genetics
  2. IRF5 gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/irf5 - Genetics
  3. PIK3R1 gene 
    ... 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( ...
    https://medlineplus.gov/genetics/gene/pik3r1 - Genetics
  4. PTPN22 gene 
    ... Health Condition MedlinePlus Genetics provides information about Systemic scleroderma More About This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/ptpn22 - Genetics
  5. PDGFRB gene 
    ... a lack of fatty tissue under the skin (lipoatrophy). This lack of fat, together with thin, wrinkled ...
    https://medlineplus.gov/genetics/gene/pdgfrb - Genetics
  6. FBN1 gene 
    ... Dietz HC. Mutations in fibrillin-1 cause congenital scleroderma: stiff skin syndrome. Sci Transl Med. 2010 Mar ...
    https://medlineplus.gov/genetics/gene/fbn1 - Genetics
  7. SLC25A24 gene 
    ... of Gorlin-Chaudhry-Moss syndrome, including skull abnormalities, lipoatrophy, and short distal phalanges, but includes normal genital ...
    https://medlineplus.gov/genetics/gene/slc25a24 - Genetics