Muir-Torre syndrome: a variant of the cancer family syndrome.

Author:

Hall N R,Williams M A,Murday V A,Newton J A,Bishop D T

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference35 articles.

1. Multiple primary carcinomata of the colon, duodenum, and larynx associated with kerato-acanthomata of the face;Muir, E.G.; Yates Bell, A.J.; Barlow, K.A.;Br J Surg; drome.'9 The colorectal cancers occurred at young age and showed a striking right sided predominance. Moreover, the occurrence of a small bowel cancer in IV-11 and a ureteric cancer in IV 12, both very rare in the general population, are characteristic of the Lynch II phenotype.22-25,1967

2. Multiple sebaceous tumours;Torre, D.;Arch Dermatol,1968

3. Multiple sebaceous neoplasms of the skin: an association with multiple visceral carcinomas, especially of the colon;Rulon, D.B.; Helwig, E.B.;Am J Clin Pathol,1973

4. Sebaceous adenoma of the eyelid and visceral malignancy;Jakobiec, F.A.;Am J Ophthalmol,1974

5. Hyperlasies sebacees, kerato-acanthomes, &pitheliomas du visage et cancer du c6lon;Reiffers, J.; Laugier, P.; Hunziker, N.;Dermatologica,1976

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