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Results 1 - 10 of 17 for acanthosis
  1. Crouzon syndrome with acanthosis nigricans is a disorder characterized by the premature joining of certain bones of the skull (craniosynostosis) during development and ...
  2. ... affected females also develop a skin condition called acanthosis nigricans, in which the skin in body folds ... as the only sign; others may also have acanthosis nigricans. In many cases, males with this condition ...
  3. SADDAN (severe achondroplasia with developmental delay and acanthosis nigricans) is a rare disorder of bone growth characterized by skeletal, brain, and skin abnormalities.All people with this condition have extremely short ...
  4. White sponge nevus is a condition characterized by the formation of white patches of tissue called nevi (singular: nevus) that appear as thickened, velvety, ...
  5. ... been identified in people with Crouzon syndrome with acanthosis nigricans. This rare condition causes premature joining of ... features. It also causes a skin abnormality called acanthosis nigricans that is characterized by thick, dark, velvety ...
  6. ... mellitus. Some people with familial partial lipodystrophy develop acanthosis nigricans, a skin condition related to high levels of insulin in the bloodstream. Acanthosis nigricans causes the skin in body folds and ...
  7. ... feet. Additionally, thick, dark, velvety areas of skin (acanthosis nigricans) are sometimes found on the hands and ... Registry: Beare-Stevenson cutis gyrata syndrome Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome National Organization for Rare Disorders ( ...
  8. ... hormonal changes. Many people with this disorder develop acanthosis nigricans, a skin condition related to high levels of insulin in the bloodstream. Acanthosis nigricans causes the skin in body folds and ...
  9. ... an increased appetite; and a skin condition called acanthosis nigricans, in which the skin in body folds ...
  10. ... skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans. Endocr Rev. 2000 Feb;21(1):23- ...
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