Syndrome of sclerodactyly, calcinosis, Raynaud's phenomenon, and telangiectasia.

Samankaltaisia teoksia

• Pulmonary capillary hemangiomatosis or hepatopulmonary syndrome in a patient with calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly and telangiectasia syndrome?
  Tekijä: Shrestha, Bijaya Laxmi, et al.
  Julkaistu: (2020)
• Primary sclerosing cholangitis associated with CREST (calcinosis, Raynaud phenomenon, oesophageal dysmotility, sclerodactyly and telangiectasia) in an elderly woman: a case report
  Tekijä: Powell, Alice, et al.
  Julkaistu: (2015)
• Dystrophic calcification in muscles of legs in calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome: Accurate evaluation of the extent with (99m)Tc-methylene diphosphonate single photon emission computed tomography/computed tomography
  Tekijä: Chakraborty, Partha Sarathi, et al.
  Julkaistu: (2015)
• Familial Raynaud's phenomenon and localized scleroderma associated with essential telangiectasia and cytogenetic abnormalities.
  Tekijä: Bunker, C B, et al.
  Julkaistu: (1990)
• Primary Raynaud's disease associated with sclerodactyly and digital osteosclerosis.
  Tekijä: Golding, D. N., et al.
  Julkaistu: (1968)