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Results 21 - 30 of 51 for Coarse features
  1. Mucolipidosis III alpha/beta 
    ... clear covering of the eye (cornea). Their facial features become slightly thickened or "coarse" over time. Affected individuals may also develop frequent ...
    https://medlineplus.gov/.../condition/mucolipidosis-iii-alpha-beta - Genetics
  2. Mucolipidosis II alpha/beta 
    ... inguinal hernia), heart valve abnormalities, distinctive-looking facial features that are described as "coarse," and overgrowth of the gums (gingival hypertrophy). Vocal ...
    https://medlineplus.gov/.../condition/mucolipidosis-ii-alpha-beta - Genetics
  3. Mucolipidosis III gamma 
    ... clear covering of the eye (cornea). Their facial features become slightly thickened or "coarse" as they get older. A small percentage of ...
    https://medlineplus.gov/genetics/condition/mucolipidosis-iii-gamma - Genetics
  4. X-linked acrogigantism 
    ... have additional signs and symptoms such as facial features that are described as coarse; disproportionately large hands or feet (acral enlargement); an ...
    https://medlineplus.gov/genetics/condition/x-linked-acrogigantism - Genetics
  5. Cantú syndrome 
    ... have a large head (macrocephaly) and distinctive facial features that are described as "coarse." These include a broad nasal bridge, skin folds ...
    https://medlineplus.gov/genetics/condition/cantu-syndrome - Genetics
  6. Multicentric osteolysis, nodulosis, and arthropathy 
    ... of the gums, heart abnormalities, and distinctive facial features that are described as "coarse." MONA is rare; its prevalence is unknown. This ...
    https://medlineplus.gov/...tric-osteolysis-nodulosis-and-arthropathy - Genetics
  7. Winchester syndrome 
    ... of the gums, heart abnormalities, and distinctive facial features that are described as "coarse." Winchester syndrome is a rare condition whose prevalence ...
    https://medlineplus.gov/genetics/condition/winchester-syndrome - Genetics
  8. Molybdenum cofactor deficiency 
    ... include a small head size (microcephaly) and facial features that are described as "coarse."Tests reveal that affected individuals have high levels ...
    https://medlineplus.gov/.../condition/molybdenum-cofactor-deficiency - Genetics
  9. SMARCB1 gene 
    ... fifth (pinky) fingers or toes, and characteristic facial features that are described as coarse. The SMARCB1 gene variants involved in Coffin-Siris ...
    https://medlineplus.gov/genetics/gene/smarcb1 - Genetics
  10. SMARCA4 gene 
    ... fifth (pinky) fingers or toes, and characteristic facial features that are described as coarse. The SMARCA4 gene variants involved in Coffin-Siris ...
    https://medlineplus.gov/genetics/gene/smarca4 - Genetics
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