• Thumbnail for Cowden syndrome
    Cowden syndrome (also known as Cowden's disease and multiple hamartoma syndrome) is an autosomal dominant inherited condition characterized by benign...
    23 KB (2,139 words) - 22:37, 10 June 2024
  • Thumbnail for Bannayan–Riley–Ruvalcaba syndrome
    polyposis syndromes, which also includes Peutz–Jeghers syndrome, juvenile polyposis and Cowden syndrome. Mutation of the PTEN gene underlies this syndrome, as...
    10 KB (759 words) - 16:51, 19 August 2024
  • Thumbnail for Hamartoma
    hamartomas include tuberous sclerosis, cowden syndrome, PTEN hamartoma tumour syndrome, and Peutz–Jeghers syndrome. About 5–8% of all solitary lung nodules...
    20 KB (1,963 words) - 07:12, 30 April 2024
  • Thumbnail for Benign tumor
    hamartoma syndrome encompasses hamartomatous disorders characterized by genetic mutations in the PTEN tumor suppressor gene, including Cowden syndrome,...
    32 KB (3,494 words) - 04:47, 14 November 2024
  • Multiple hamartoma syndrome is a syndrome characterized by more than one hamartoma.: 673  It is sometimes equated with Cowden syndrome. However, MeSH also...
    2 KB (110 words) - 23:49, 7 July 2024
  • Thumbnail for Birt–Hogg–Dubé syndrome
    the similarity in phenotype between BHD syndrome, Cowden syndrome, tuberous sclerosis, and Peutz–Jeghers syndrome. Most of the cancer-causing mutations...
    41 KB (4,456 words) - 11:44, 18 May 2024
  • Thumbnail for Polyp (medicine)
    syndrome Turcot syndrome Juvenile polyposis syndrome Cowden disease Bannayan–Riley–Ruvalcaba syndrome (Bannayan–Zonana syndrome) Gardner's syndrome Serrated...
    26 KB (2,441 words) - 22:48, 11 September 2024
  • fever Cowden syndrome Cracked tooth syndrome Cramp fasciculation syndrome Crandall syndrome Craniosynostosis–anal anomalies–porokeratosis syndrome...
    42 KB (4,068 words) - 16:56, 1 November 2024
  • Thumbnail for Lipomatosis
    entities which are accompanied by multiple lipomas include Proteus syndrome, Cowden syndrome and related disorders due to PTEN gene mutations, benign symmetric...
    5 KB (433 words) - 19:48, 30 October 2024
  • Thumbnail for Human head
    of cancer in individuals who carry the genetic mutation that causes Cowden syndrome. For adults, this refers to head sizes greater than 58 centimeters...
    11 KB (1,302 words) - 03:34, 17 November 2024
  • Thumbnail for Macrocephaly
    Cowden disease, neurofibromatosis type 1, and tuberous sclerosis; overgrowth syndromes such as Sotos syndrome (cerebral gigantism), Weaver syndrome,...
    18 KB (1,723 words) - 11:31, 16 September 2024
  • of hormones produced in vertebrates, and their synthetic analogues Cowden syndrome, a rare autosomal dominant inherited disorder (-)-camphene synthase...
    6 KB (688 words) - 04:04, 15 September 2024
  • Thumbnail for Trichilemmoma
    associated with Cowden syndrome, in which hamartomatous intestinal polyposis is seen in conjunction with multiple tricholemmoma lesions. Cowden syndrome Trichilemmal...
    2 KB (133 words) - 05:36, 17 December 2020
  • Thumbnail for Lhermitte–Duclos disease
    the granular layer of the cerebellum. It is often associated with Cowden syndrome. It was described by Jacques Jean Lhermitte and P. Duclos in 1920....
    6 KB (520 words) - 18:07, 11 October 2024
  • Thumbnail for Uterine cancer
    use, late menopause, and certain hereditary conditions (Lynch syndrome, Cowden syndrome). Risk factors for uterine sarcoma include prior radiation therapy...
    25 KB (2,040 words) - 12:02, 4 November 2024
  • Australian actress All pages with titles containing Cowden Cowden Park House Cowden syndrome Cowden v. Commissioner, a case in the 1961 United States Court...
    1 KB (151 words) - 00:10, 11 September 2024
  • Jordan's syndrome (JS) or PPP2R5D-related intellectual disability is a rare autosomal dominant neurodevelopmental disorder caused by de novo mutations...
    9 KB (791 words) - 03:21, 10 February 2024
  • Thumbnail for Male breast cancer
    other rare inherited genetic disorders, the Li-Fraumeni syndrome, Lynch syndrome, and Cowden syndrome, although the odds ratios (i.e. statistical strength)...
    37 KB (4,652 words) - 07:15, 9 June 2024
  • Thumbnail for Hereditary breast–ovarian cancer syndrome
    cancer under age 30 have a mutation in this gene. PTEN: Mutations cause Cowden syndrome, which produces hamartomas (benign polyps) in the colon, skin growths...
    11 KB (1,135 words) - 17:29, 17 September 2024
  • Thumbnail for SDHD
    gene have been identified in people with Cowden syndrome or a similar disorder called Cowden-like syndrome. These conditions are characterized by multiple...
    21 KB (2,718 words) - 06:22, 3 June 2024
  • Thumbnail for Micrognathism
    severe fetal Cornelia de Lange syndrome 1, 3, and 5 Costello syndrome Cowden syndrome 5 and 6 Cranioectodermal dysplasia 2 and 3 Craniofacial microsomia...
    14 KB (1,343 words) - 23:07, 16 October 2024
  • RV, Turner S, Ledbetter DH, Martin CL (1993). "17q12 Recurrent Deletion Syndrome". In Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Stephens K, Amemiya...
    43 KB (995 words) - 08:29, 11 November 2024
  • Thumbnail for PTEN (gene)
    identified more than 70 mutations in the PTEN gene in people with Cowden syndrome.[citation needed] These mutations can be changes in a small number...
    30 KB (3,405 words) - 21:19, 21 August 2024
  • Thumbnail for Juvenile polyposis syndrome
    syndrome but are actually affected with Cowden syndrome or other phenotypes of the PTEN hamartoma tumor syndrome. Mutations in SMAD4 may be additionally...
    7 KB (620 words) - 23:11, 7 June 2024
  • Thumbnail for Thyroid cancer
    in women with familial adenomatous polyposis and in patients with Cowden syndrome. A follicular variant of papillary thyroid cancer also exists. Newly...
    59 KB (5,283 words) - 06:14, 11 November 2024
  • Thumbnail for Hereditary cancer syndrome
    [citation needed] Birt–Hogg–Dubé syndrome, Carney syndrome, familial chordoma, Cowden syndrome, dysplastic nevus syndrome with familial melanoma, familial...
    51 KB (5,582 words) - 14:19, 15 July 2024
  • Thumbnail for Leser–Trélat sign
    papillomatosis, ichthyosis acquisita (acquired hypertrichosis lanuginosa), Cowden syndrome, tylosis, acrokeratosis paraneoplastica of Bazex or tripe palms accompany...
    5 KB (466 words) - 02:24, 8 August 2024
  • Thumbnail for Genetic testing
    sarcoma, osteosarcoma (bone cancer), leukemia and brain tumors. In the Cowden syndrome there is a mutation on the PTEN gene, causing potential breast, thyroid...
    56 KB (6,621 words) - 00:59, 18 November 2024
  • Thumbnail for Breast cancer
    developing breast cancer, namely p53 (causes Li–Fraumeni syndrome), PTEN (causes Cowden syndrome), and PALB1. Breast changes like atypical ductal hyperplasia...
    134 KB (15,172 words) - 09:52, 13 November 2024
  • Thumbnail for Fissured tongue
    healthy individuals. Fissured tongue is also sometimes a feature of Cowden's syndrome. The cause is unknown, but is most likely a genetic trait. Aging and...
    5 KB (422 words) - 20:33, 13 November 2023