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2015, Number 3

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Rev Med MD 2015; 6.7 (3)

Gorlin-Goltz syndrome: A clinical case presentation

Villegas-Pacheco J, Mojica-Padilla LA, López-Reyes SL, Arias-Patiño JJG

Language: Spanish
References: 10
Page: 227-230
PDF size: 846.81 Kb.


ABSTRACT

The Gorlin-Goltz syndrome or Basal Cell Nevus is an ectodermic neoplasia, hereditary and autosomal dominantly by the mutation of PTCH1 genes in the 9q22 chromosome; PTCH2 gene 1p32 or the SUFU gene in 10q24-q25. It is a multi systemic rare disease with a prevalence of 1 in 57,000 to 150,000 people. It is characterized by the presence of multiple Basal Cell Nevus carcinomas, development of keratocystic odontogenic tumors, pits or palmoplantar dimples.


REFERENCES

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