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Results 1 - 10 of 16 for Cowden syndrome
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  1. Cowden syndrome is a genetic disorder characterized by multiple noncancerous, tumor-like growths called hamartomas and an increased risk of developing certain ...
  2. ... WWP1 gene have been identified in people with Cowden syndrome or a similar disorder called Cowden-like syndrome. ... the uterine lining (endometrial cancer). Other features of Cowden syndrome can include an enlarged head (macrocephaly) and a ...
  3. ... cases, this increased risk occurs as part of Cowden syndrome (described below). Inherited mutations in the PTEN gene ... mutations in the PTEN gene that can cause Cowden syndrome or a similar disorder called Cowden-like syndrome. ...
  4. ... syndrome overlap with those of another disorder called Cowden syndrome. People with Cowden syndrome develop hamartomas and other noncancerous growths; they also ...
  5. ... to be a tumor suppressor. Some cases of Cowden syndrome and a similar condition called Cowden-like syndrome ... an increased risk of developing certain cancers. When Cowden syndrome and Cowden-like syndrome are caused by KLLN ...
  6. ... This Health Condition MedlinePlus Genetics provides information about Cowden syndrome More About This Health Condition The SDHB gene ... breast and thyroid cancer risks in Cowden and Cowden-like syndrome via FAD/NAD-dependant destabilization of p53. Hum ...
  7. ... This Health Condition MedlinePlus Genetics provides information about Cowden syndrome More About This Health Condition CBT1 CII-4 ... breast and thyroid cancer risks in Cowden and Cowden-like syndrome via FAD/NAD-dependant destabilization of p53. Hum ...
  8. ... and counseling for BRCA1 and BRCA2, Lynch syndrome, Cowden syndrome, and Li-Fraumeni syndrome. Obstet Gynecol Clin North ...
  9. ... and counseling for BRCA1 and BRCA2, Lynch syndrome, Cowden syndrome, and Li-Fraumeni syndrome. Obstet Gynecol Clin North ...
  10. ... and counseling for BRCA1 and BRCA2, Lynch syndrome, Cowden syndrome, and Li-Fraumeni syndrome. Obstet Gynecol Clin North ...
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