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Cowden syndrome

also listed as Multiple Hamartoma syndrome

6 people found, showing 1 to 6

To save room on the page we use the term disabled to indicate those with disabilities, special need or a medical condition.


Birmingham ( West Midlands )

Nov 2013  not given
Family type: two parent family
Siblings: 0
Disabled siblings: 5
Username: daddysgirl10
Relationship: Female
Other conditions: None

Last updated: 03 Nov 2013
Brief summary: im from a family with cowden syndrome, its runs in my fathers genes its past from my father to my brother and 3 sisters out of my dads children im the only child who does not have cowden syndrome, I find it very difficult talking about this condition.

Bromley ( London Boroughs )

Sep 2008  male
Family type: two parent family
Siblings: 1
Disabled siblings: 0
Username: Tobysmum76
Relationship: Mother
Last updated: 17 Jul 2013
Brief summary: My son has Cowden syndrome, which in him has caused global developmental delay with severe communication difficulties.


May 2013  female
Family type: two parent family
Siblings: 1
Disabled siblings: 0
Username: Sedge37
Relationship: Mother
Last updated: 20 Aug 2015
Brief summary: 2 Year Old Daughter diagnosed with PTEN Harmatoma Tumour Syndrome.

Northamptonshire ( East Midlands )

Dec 2007  male
Family type: single parent family
Siblings: 1
Disabled siblings: 1
Username: wilson12
Relationship: Mother
Last updated: 04 Nov 2011
Brief summary: He has BRRS, Cowden syndrome. His symptoms are: large head, low muscle tone, severe developmental delay, autistic spectrum disorder.

Northumberland ( North East Region )

Dec 2003  male
Family type: two parent family
Siblings: 2
Disabled siblings: 2
Username: kirthomp
Relationship: Mother
Other conditions: None

Last updated: 18 Apr 2012
Brief summary: I am the mum of 2 children with Cowden syndrome a PTEN genetic disorder. My son has had Thyroid cancer and has autism. My daughter has vascular malformations and has recently had a prophelactic thyroidectomy,

Yorkshire and the Humber ( England )

Feb 2006  male
Family type: two parent family
Siblings: 2
Disabled siblings: 1
Username: jammie130
Relationship: Mother
Last updated: 06 Nov 2016
Brief summary: We have 3 kids, they eldest has inherited the pten mutation from his dad so is diagnosed Bannayan-Riley-ruvalcaba or Cowden's syndrome.

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Benign Spinal Cord Tumour (Spinal Cord Tumour) 0 -
Bone Tumour 0 -
Brain Tumour (PNET; Apendeoma; Pilocystic Astrocytoma) 12 G
Carcinoid disease (Carcinoid syndrome) 0 -
Craniopharyngioma 0 -
Desmoid Tumour (Musculo-aponeurotic fibromatosis; aponeurotic fibromatosis; agressive fibromatosis) 1 -
Dysembryoplastic Neuroepithelial Tumour 2 -
Epithelioid Haemangioendothelioma 0 -
Glomangioma (angiomyoneuroma; angioneuroma) 1 -
Juvenile Angiofibroma (Angiofibroma; Juvenile Nasopharyngeal Angiofibroma) 0 -
Medulloblastoma 2 -
Multiple Epitheliomata 0 -
Phaeochromocytoma 0 -
Pheochromocytoma 0 -
Pilocystic Astrocytoma 0 -
Pinealoma 0 -
Rhabdomyoma 2 -
Syringoma 0 -

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