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Results 1 - 10 of 20 for Abnormality of skin pigmentation
  1. ... is a condition that causes a variety of abnormalities involving bone development, skin coloring (pigmentation), and fat distribution. People with this condition may ...
  2. ... hair; malformations of the fingernails and toenails; and abnormalities of skin coloring (pigmentation), such as light brown patches called café-au-lait spots.Coats plus syndrome and a disorder called leukoencephalopathy with ... However, researchers recently found that Coats plus syndrome ...
  3. ... they are needed for the development of normal skin pigmentation. This disruption of melanosome transport is thought to cause the pigmentation abnormalities seen in individuals with Dowling-Degos disease.Mutations ...
  4. ... syndrome include short stature, seizures, heart defects, and abnormalities of the urinary tract and genitalia. Less commonly, this condition also affects the eyes, teeth, hands, and skin coloring (pigmentation). Although many different medical issues have been associated ...
  5. ... scalp (dermal hypoplasia or aplasia), and changes in skin coloring (pigmentation) are also possible.The most common eye abnormality in ECCL is a noncancerous growth called a ...
  6. ... may develop areas of abnormally light or dark skin coloring (pigmentation).Many individuals with MOPDII have blood vessel abnormalities. For example, some affected individuals develop a bulge ...
  7. ... SJS/TEN can include changes in skin coloring (pigmentation), dryness of the ... abnormalities. A small percentage of affected individuals develop chronic ...
  8. ... 1 is a condition characterized by changes in skin coloring (pigmentation) and the growth of tumors along nerves in ... stature, an unusually large head (macrocephaly), and skeletal abnormalities such as an abnormal curvature of the spine ( ...
  9. ... the normal growth of skull bones and affects skin pigmentation. These changes lead to the features of Crouzon syndrome with acanthosis nigricans. ... Citation on PubMed
  10. ... of keratin 14 is related to changes in skin pigmentation. KRT14 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. ... Epub 2007 Nov 29. Citation on PubMed
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