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P.207 Diagnosis and treatment of patients with nevoid basal cell carcinoma syndrome (Gorlin-Goltz-Syndrome)

✍ Scribed by R.E. Friedrich


Book ID
119581144
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
62 KB
Volume
34
Category
Article
ISSN
1010-5182

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## Mutations in the PTCH gene, the human homolog of the Drosophila patched gene, have been found to lead to the autosomal dominant disorder termed Nevoid Basal Cell Carcinoma Syndrome (NBCCS, also called Gorlin Syndrome). Patients display an array of developmental anomalies and are prone to develop