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MLH1
LE WE PMID CA
MLH113007MLH1

Basal cell carcinoma

Basaloid follicular hamartoma

Bazex acrokeratosis paraneoplastica

Birt Hogg Dube syndrome

Brooke Spiegler syndrome

Colon and rectum (Neoplasia)

Cowden s syndrome

CYLD Cylindromatosis

Familial cylindromatosis

Fibrofolliculoma

FLCN Folliculin

Generalised basaloid follicular hamartoma syndrome

Genetics (Microsatellite)

Gorlin Goltz phacomatosis Gorlin s syndrome Naevoid basal cell carcinoma

Keratoacanthoma

Lynch syndrome

MLH1

Mltiple familial trichoepitheliomas

MSH2

MSH6

Muir Torre s syndrome

Neoplasia (Inherited)

PMS2

PTCH

PTEN MMAC1 TEP1

Seabceous epithelioma

Sebaceous adenoma

Sebaceous carcinoma

Skin (Neoplasia)

Spiradenoma

Trichilemmoma

Trichodiscoma

Trichoepithelioma

2010  
1
Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers.
[20587412] J Med Genet 47(9): 579-85 (2010)
2005  
2
Genetics of skin appendage neoplasms and related syndromes.
[16272260] J Med Genet 42(11): 811-9 (2005)
2011  
3
Evidence for classification of c.1852_1853AA>GC in MLH1 as a neutral variant for Lynch syndrome.
[21247423] BMC Med Genet 12(-): 12 (2011)

Downloaded from http://www.kidney.de - The Database of Free Medical Reviews - The Metatextbook of Medicine - Ossip Groth

All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.


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