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Results 1 - 10 of 10 for dermatomyositis OR poikiloderma OR shawl sign
  1. Baller-Gerold syndrome 
    ... These chronic skin problems are collectively known as poikiloderma.The varied signs and symptoms of Baller-Gerold syndrome overlap with ...
    https://medlineplus.gov/genetics/condition/baller-gerold-syndrome - Genetics
  2. Rothmund-Thomson syndrome 
    ... mutated gene, but they typically do not show signs and symptoms of the condition. Congenital poikiloderma Poikiloderma atrophicans and cataract Poikiloderma congenitale Poikiloderma congenitale ...
    https://medlineplus.gov/genetics/condition/rothmund-thomson-syndrome - Genetics
  3. Poikiloderma with neutropenia 
    ... mutated gene, but they typically do not show signs and symptoms of the condition. Clericuzio type poikiloderma with neutropenia Immune-deficient poikiloderma Poikiloderma with neutropenia, ...
    https://medlineplus.gov/.../condition/poikiloderma-with-neutropenia - Genetics
  4. Kindler epidermolysis bullosa 
    ... altered gene, but they typically do not show signs and symptoms of the condition. Congenital bullous poikiloderma Kindler syndrome Kindler's syndrome Poikiloderma of Kindler ...
    https://medlineplus.gov/.../condition/kindler-epidermolysis-bullosa - Genetics
  5. Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis 
    Hereditary fibrosing poikiloderma ... individuals.People with POIKTMP have patchy changes in skin coloring and small clusters ...
    https://medlineplus.gov/...tractures-myopathy-and-pulmonary-fibrosis - Genetics
  6. Systemic scleroderma 
    ... people with features of systemic scleroderma also have signs and symptoms of another condition that affects connective tissue, such as polymyositis, dermatomyositis, rheumatoid arthritis, Sjögren syndrome, or systemic lupus erythematosus. ...
    https://medlineplus.gov/genetics/condition/systemic-scleroderma - Genetics
  7. IFIH1 gene 
    ... against others. AGS7 CADM-140 autoantigen clinically amyopathic dermatomyositis autoantigen 140 kDa DEAD/H (Asp-Glu-Ala- ...
    https://medlineplus.gov/genetics/gene/ifih1 - Genetics
  8. USB1 gene 
    ... USB1 gene have been identified in people with poikiloderma with neutropenia (PN). This condition involves a group of skin abnormalities called poikiloderma and a persistent shortage (deficiency) of neutrophils (chronic ...
    https://medlineplus.gov/genetics/gene/usb1 - Genetics
  9. FAM111B gene 
    ... have been identified in people with hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis (POIKTMP). ... S. Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due ...
    https://medlineplus.gov/genetics/gene/fam111b - Genetics
  10. Aarskog-Scott syndrome 
    ... Most males with Aarskog-Scott syndrome have a shawl scrotum, in which the scrotum surrounds the penis ... copy of the FGD1 gene may show mild signs of the condition, such as hypertelorism, short stature, ...
    https://medlineplus.gov/genetics/condition/aarskog-scott-syndrome - Genetics