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Results 1 - 10 of 17 for Dyskeratosis "congenita," "X-linked"
  1. Dyskeratosis congenita 
    Dyskeratosis congenita is a disorder that can affect many parts of the body. There are three features that ... patches inside the mouth (oral leukoplakia).People with dyskeratosis congenita have an increased risk of developing several life- ...
    https://medlineplus.gov/genetics/condition/dyskeratosis-congenita - Genetics
  2. DKC1 gene 
    ... DKC1 gene have been identified in people with dyskeratosis congenita. This disorder is characterized by changes in skin ... formed fingernails and toenails (nail dystrophy). People with dyskeratosis congenita have an increased risk of developing several life- ...
    https://medlineplus.gov/genetics/gene/dkc1 - Genetics
  3. TERT gene 
    ... TERT gene have been identified in people with dyskeratosis congenita. This disorder is characterized by changes in skin ... formed fingernails and toenails (nail dystrophy). People with dyskeratosis congenita have an increased risk of developing several life- ...
    https://medlineplus.gov/genetics/gene/tert - Genetics
  4. TINF2 gene 
    ... TINF2 gene have been identified in people with dyskeratosis congenita, including a severe form of this disorder called Revesz syndrome. Dyskeratosis congenita is characterized by changes in skin coloring (pigmentation), ...
    https://medlineplus.gov/genetics/gene/tinf2 - Genetics
  5. TERC gene 
    ... TERC gene have been identified in people with dyskeratosis congenita. This disorder is characterized by changes in skin ... formed fingernails and toenails (nail dystrophy). People with dyskeratosis congenita have an increased risk of developing several life- ...
    https://medlineplus.gov/genetics/gene/terc - Genetics
  6. Skin Conditions (National Library of Medicine)  
    What does your skin do? Your skin is your body's largest organ. It covers the entire outside of your body. There are many ways that your skin protects ...
    https://medlineplus.gov/skinconditions.html - Health Topics
  7. Patient support and advocacy groups 
    ... Deficiency Foundation Dup 15q Alliance Dupuytren Research Group Dyskeratosis Congenita Outreach EA/TEF Child and Family Support Connection ...
    https://medlineplus.gov/about/general/genetics/supportadvocacygroups -
  8. Poikiloderma with neutropenia 
    ... length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund-Thomson syndrome. Hum ...
    https://medlineplus.gov/.../condition/poikiloderma-with-neutropenia - Genetics
  9. CTC1 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Dyskeratosis congenita More About This Health Condition AAF-132 AAF132 ...
    https://medlineplus.gov/genetics/gene/ctc1 - Genetics
  10. USB1 gene 
    ... length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund-Thomson syndrome. Hum ...
    https://medlineplus.gov/genetics/gene/usb1 - Genetics
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