Familial Cylindromatosis
Common Name(s)
Familial Cylindromatosis, Turban tumor syndrome
Advocacy and Support Organizations
Condition Specific Organizations
Following organizations serve the condition "Familial Cylindromatosis" for support, advocacy or research.
How do you compare to others with this condition?
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Advocacy and Support Organizations
Condition Specific Organizations
Following organizations serve the condition "Familial Cylindromatosis" for support, advocacy or research.
Recommended Apps
Anonymously share and see how your answers compare with others with this condition while privately providing key pieces of information to medical researchers, disease advocacy groups, and others ONLY YOU select to help speed up cures and better alternatives.
Finding the right clinical trial for Familial Cylindromatosis can be challenging. However, with TrialsFinder (which uses the Reg4ALL database and privacy controls by Private Access), you can permit researchers to let you know opportunities to consider - all without revealing your identity.
Scientific Literature
Articles from the PubMed Database
Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Familial Cylindromatosis" returned 7 free, full-text research articles on human participants.
First 3 results:
Journal:
Multiple familial trichoepithelioma type 1 (MFT1; MIM 601606), a rare monogenic skin disease with autosomal dominant inheritance, is characterized by the development of multiple skin-colored papules on the central area of the face, frequently occurring in the nasolabial area. The ...
Journal: Fam. Cancer. 2011 Mar;10(1):127-32.
Pathogenic mutations in CYLD can be identified in patients affected with Brooke-Spiegler syndrome, (Familial) Cylindromatosis or multiple familial trichoepithelioma. To date, only technologies which are able to identify small point mutations in CYLD, such as sequence and WAVE analysis, ...
Journal: J. Invest. Dermatol.. 2005 May;124(5):919-20.
Brooke-Spiegler syndrome (BSS), familial cylindromatosis (FC), and multiple familial trichoepithelioma (MFT), originally described as distinct entities, share overlapping clinical findings. Patients with BSS are predisposed to multiple skin appendage tumors such as cylindroma, trichoepithelioma, ...
To view other free, full-text articles on human participants, please click on the link below.
Reviews from the PubMed Database
Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Familial Cylindromatosis" returned 0 free, full-text review articles on human participants.
No free, full-text review articles on human participants are available at this time. Please click this link to visit the PubMed website for results on "Familial Cylindromatosis".
Symptoms, Diagnosis, and Treatment
https://ghr.nlm.nih.gov/gene/TRAIP
https://ghr.nlm.nih.gov/condition/multiple-familial-trichoepithelioma
https://ghr.nlm.nih.gov/gene/CYLD
https://ghr.nlm.nih.gov/condition/familial-hypobetalipoproteinemia
https://ghr.nlm.nih.gov/condition/familial-hyperaldosteronism
https://ghr.nlm.nih.gov/condition/familial-candidiasis
https://ghr.nlm.nih.gov/condition/familial-erythrocytosis
https://ghr.nlm.nih.gov/condition/familial-dysautonomia
https://ghr.nlm.nih.gov/condition/familial-porencephaly
https://ghr.nlm.nih.gov/condition/familial-hemiplegic-migraine
https://ghr.nlm.nih.gov/condition/familial-hypertrophic-cardiomyopathy
https://ghr.nlm.nih.gov/condition/familial-hemophagocytic-lymphohistiocytosis
https://ghr.nlm.nih.gov/condition/familial-hdl-deficiency
https://ghr.nlm.nih.gov/condition/familial-cold-autoinflammatory-syndrome
https://ghr.nlm.nih.gov/condition/familial-exudative-vitreoretinopathy
https://ghr.nlm.nih.gov/condition/familial-isolated-hyperparathyroidism
https://ghr.nlm.nih.gov/condition/familial-isolated-pituitary-adenoma
https://ghr.nlm.nih.gov/condition/familial-dilated-cardiomyopathy
https://ghr.nlm.nih.gov/condition/familial-lipoprotein-lipase-deficiency
There are currently no related results available in GeneReviews.
Clinical Trial Information This information is provided by ClinicalTrials.gov
There are currently no open clinical trials for this condition.
Finding the right clinical trial for Familial Cylindromatosis can be challenging. However, with TrialsFinder (which uses the Reg4ALL database and privacy controls by Private Access), you can permit researchers to let you know opportunities to consider - all without revealing your identity.