Familial Dysplastic Naevus Syndrome

Norris W. A case of fungoid disease. Edinb Med Surg J 1820; 16: 562–5

Munro D.D. Multiple active junctional naevi with a family history of malignant melanoma. Proc R Soc Med 1974; 67: 594–5

Clark W.H. , Reimer R.R. , Greene M. , Ainsworth A.M. , Mastrangelo M.J. Origin of familial malignant melanomas from heritable melanocyte lesions ‘the BK mole syndrome’. Arch Dermatol 1978; 114: 732–8

Lynch H. , Frichot B.C. , Lynch J. Familial atypical multiple mole melanoma syndrome. J Med Genet 1978; 15: 352–6

Mackie R.M. Multiple melanoma and atypical melanocyte naevi - evidence of an activated and expanded melanocyte system. Br J Dermatol 1982; 107: 621–9

Greene M.H. , Goldin L.R. , Clark W.H. , Lovrien E. , Kraemer K.R. , Tucker M.A. , Elder D.E. , Fraser M.C. , Rowe S. Familial cutaneous melanoma: Autosomal dominant trait possibly linked to the Rh locus. Proc Natl Acad Sci USA 1983; 80: 6071–5

Elder D.E. , Goldman L.I. , Goldman S.C. , Greene M.H. , Clark W.H. Dysplastic nevus syndrome: a phenotypic association of sporadic cutaneous melanoma. Cancer 1980; 46: 1787–94

Kraemer K.H. , Greene M.H. , Tarone R. , Elder D.E. , Clark W.H. , Guerry D. Dysplastic naevi and cutaneous melanoma risk. Lancet 1983; ii: 1076–7

Mackie R.M. , English J.S.C. Ashworth J, Doherty V. Managing the dysplastic naevus. Lancet 1983; ii: 1249–50

Greene M.H. , Clark W.H. , Tucker M.A. , Elder D.E. , Kraemer K.H. , Guerry D. , Fraser M.C. Managing the dysplastic naevus syndrome. Lancet 1984; i: 166–7

Lynch H.T. , Fusaro R.M. , Pester J. . Tumour spectrum in the FAMM syndrome. Br J Cancer 1981; 44: 553–60

Adams S.J. , Rustin M.H.A. , Robinson T.W.E. , Munro D.D. The dysplastic naevus syndrome and endocrine disease. Br Med J 1984; 288: 1790–1.