The nevoid basal cell carcinoma syndrome (NBCCS) or Gorlin - Goltz syndrome is an autosomal disorder principally characterized by cutaneous basal cell carcinomas, multiple keratocysts, and skeletal anomalies. The major organ systems involved are skin, bones, central nervous system, eyes, gonads and endocrine. This particular syndrome is extensively described in the literature under different names. However, there are only few cases reported in the Indian literature. An unusual case of a 33-year old male with large odontogenic keratocyst involving impacted canine in the mandible, along with multiple cysts and impacted teeth in the maxilla; bifid rib and vertebral anomalies has been described
BACKGROUND: The Nevoid Basal Cell Carcinoma Syndrome (NBCCS) or Gorlin-Goltz Syndrome (GGS) is a gen...
The nevoid basal cell carcinoma syndrome, or Gorlin-Goltz syndrome, is an autosomal dominant multipl...
Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon autosomal dominant in...
The nevoid basal cell carcinoma syndrome (NBCCS) or Gorlin-Goltz Syndrome is an autosomal dominant d...
The Nevoid Basal-Cell Carcinoma Syndrome (NBCC), or as it is also referred to, basal-cell nevus synd...
Gorlin-Goltz syndrome or nevoid basal cell carcinoma syndrome (NBCCS) comprises multiple basal cell ...
Nevoid basal cell carcinoma syndrome (BCNS) is an autosomal dominant inherited disorder. Multiple or...
Nevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant inherited condition that exhib...
The Nevoid Basal-Cell Carcinoma Syndrome (NBCC), or as it is also referred to, basal-cell nevus synd...
Nevoid basal cell carcinoma syndrome (NBCC; Gorlin syndrome), an autosomal dominant disorder linked ...
Nevoid basal cell carcinoma syndrome (NBCCS) is a hereditary condition transmitted as an autosomal d...
Nevoid basal cell carcinoma syndrome (also named Gorlin-Goltz syndrome) is a rare disease. Commonly ...
The major features of the nevoid basal-cell carcinoma syndrome are epidermal multiple cell carcinoma...
One hundred eighteen cases of nevoid basal cell carcinoma syndrome (NBCCS, Gorlin's syndrome or basa...
Nevoid basal cell carcinoma syndrome (NBCCS) is a hereditary condition transmitted as an autosomal d...
BACKGROUND: The Nevoid Basal Cell Carcinoma Syndrome (NBCCS) or Gorlin-Goltz Syndrome (GGS) is a gen...
The nevoid basal cell carcinoma syndrome, or Gorlin-Goltz syndrome, is an autosomal dominant multipl...
Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon autosomal dominant in...
The nevoid basal cell carcinoma syndrome (NBCCS) or Gorlin-Goltz Syndrome is an autosomal dominant d...
The Nevoid Basal-Cell Carcinoma Syndrome (NBCC), or as it is also referred to, basal-cell nevus synd...
Gorlin-Goltz syndrome or nevoid basal cell carcinoma syndrome (NBCCS) comprises multiple basal cell ...
Nevoid basal cell carcinoma syndrome (BCNS) is an autosomal dominant inherited disorder. Multiple or...
Nevoid basal cell carcinoma syndrome (NBCCS) is an autosomal dominant inherited condition that exhib...
The Nevoid Basal-Cell Carcinoma Syndrome (NBCC), or as it is also referred to, basal-cell nevus synd...
Nevoid basal cell carcinoma syndrome (NBCC; Gorlin syndrome), an autosomal dominant disorder linked ...
Nevoid basal cell carcinoma syndrome (NBCCS) is a hereditary condition transmitted as an autosomal d...
Nevoid basal cell carcinoma syndrome (also named Gorlin-Goltz syndrome) is a rare disease. Commonly ...
The major features of the nevoid basal-cell carcinoma syndrome are epidermal multiple cell carcinoma...
One hundred eighteen cases of nevoid basal cell carcinoma syndrome (NBCCS, Gorlin's syndrome or basa...
Nevoid basal cell carcinoma syndrome (NBCCS) is a hereditary condition transmitted as an autosomal d...
BACKGROUND: The Nevoid Basal Cell Carcinoma Syndrome (NBCCS) or Gorlin-Goltz Syndrome (GGS) is a gen...
The nevoid basal cell carcinoma syndrome, or Gorlin-Goltz syndrome, is an autosomal dominant multipl...
Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon autosomal dominant in...