Scholarlink

Cronkhite–Canada syndrome is characterized by a constellation of clinical features that includes generalized gastrointestinal polyposis, skin hyperpigmentation, alopecia, and onychatrophia. The condition is not familial. The etiology is unknown. There is no consistently effective treatment.

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Cronkhite–Canada Syndrome

  • 章节

  • 发表日期：

    2025年

查看全文
  • Jessica R. Philpott,
  • Carolyn L. Power,
  • Eric W. Willis,
  • Robert S. O’Shea,
  • Michelle D. Inkster,
  • James S. Wu

摘要

Cronkhite–Canada syndrome is characterized by a constellation of clinical features that includes generalized gastrointestinal polyposis, skin hyperpigmentation, alopecia, and onychatrophia. The condition is not familial. The etiology is unknown. There is no consistently effective treatment.