Acanthosis nigricans in a Chinese girl with FGFR3 K650 T mutation: a case report and literature review
Abstract Background Acanthosis nigricans (AN) is a clinical manifestation featured by velvety brown plaques in skin folds that occurs in some hereditary and syndromic disorders. Fibroblast growth factor receptor 3 (FGFR3) mutations have been identified as one of the genetic causes of inherited AN. C...
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| Main Authors: | , , , , |
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| Format: | Book |
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BMC,
2019-01-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |