Add to ORKGGorlin-Goltz syndrome, also known as nevoid basal cell carcicoma syndrome, comes into being due to a genetic alteration produced by a mutation in the ?Patched? tumour suppressor gene, and it is inherited in a dominant autosomal way, though sporadic cases have been found. This syndrome shows a high penetrance and variable expressiveness. It is about a multisystemic process that is characterised by the presence of multiple pigmented basocellular carcinomas, keratocysts in the jaws, palmar and/or plantar pits and calcification of the falxcerebri. Together with these major features a great number of processes considered as minor features have also been described. The latter include numerous skeletical, dermatology related and neurological...
Gorlin syndrome is a rare autosomal dominant disorder exhibiting high penetrance and variable expres...
Gorlin-Goltz syndrome (GGS) is a rare autosomal dominant disorder. The disease shows multiple organ ...
Gorlin-Goltz syndrome (SGG) is a rare autosomal dominant disorder. Although it is hereditary, there ...
Gorlin-Goltz syndrome, also known as nevoid basal cell carcicoma syndrome, comes into being due to a...
Gorlin-Goltz syndrome, also known as nevoid basal cell carcicoma syndrome, comes into being due to a...
Gorlin-Goltz syndrome is uncommon multisystemic disease with an autosomal dominant trait, with compl...
Gorlin-Goltz syndrome or nevoid basal cell carcinoma syndrome is a rare hereditary autosomal-dominan...
Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon autosomal dominant in...
Gorlin and Goltz syndrome are a very complex syndrome and a multisystemic process that is characteri...
Gorlin Goltz syndrome (GGS) is a rare syndrome caused due to inheritance of autosomal dominant gene ...
Background: Gorlin-Goltz syndrome, also known as nevoid basal cell carcinoma syndrome, is a rare gen...
Nevoid basal cell carcinoma syndrome (Gorlin syndrome) is an autosomal dominant inherited condition ...
The Gorlin-Goltz syndrome, nevoid basal cell carcinoma syndrome, or basal cell nevus syndrome is an ...
Objectives. Gorlin-Goltz syndrome (GGS) is a rare autosomal dominant disorder. The disease shows mul...
The Gorlin-Goltz syndrome is an infrequent multisystemic disease, which is inherited in an autosomal...
Gorlin syndrome is a rare autosomal dominant disorder exhibiting high penetrance and variable expres...
Gorlin-Goltz syndrome (GGS) is a rare autosomal dominant disorder. The disease shows multiple organ ...
Gorlin-Goltz syndrome (SGG) is a rare autosomal dominant disorder. Although it is hereditary, there ...
Gorlin-Goltz syndrome, also known as nevoid basal cell carcicoma syndrome, comes into being due to a...
Gorlin-Goltz syndrome, also known as nevoid basal cell carcicoma syndrome, comes into being due to a...
Gorlin-Goltz syndrome is uncommon multisystemic disease with an autosomal dominant trait, with compl...
Gorlin-Goltz syndrome or nevoid basal cell carcinoma syndrome is a rare hereditary autosomal-dominan...
Gorlin-Goltz syndrome, also known as basal cell nevus syndrome, is an uncommon autosomal dominant in...
Gorlin and Goltz syndrome are a very complex syndrome and a multisystemic process that is characteri...
Gorlin Goltz syndrome (GGS) is a rare syndrome caused due to inheritance of autosomal dominant gene ...
Background: Gorlin-Goltz syndrome, also known as nevoid basal cell carcinoma syndrome, is a rare gen...
Nevoid basal cell carcinoma syndrome (Gorlin syndrome) is an autosomal dominant inherited condition ...
The Gorlin-Goltz syndrome, nevoid basal cell carcinoma syndrome, or basal cell nevus syndrome is an ...
Objectives. Gorlin-Goltz syndrome (GGS) is a rare autosomal dominant disorder. The disease shows mul...
The Gorlin-Goltz syndrome is an infrequent multisystemic disease, which is inherited in an autosomal...
Gorlin syndrome is a rare autosomal dominant disorder exhibiting high penetrance and variable expres...
Gorlin-Goltz syndrome (GGS) is a rare autosomal dominant disorder. The disease shows multiple organ ...
Gorlin-Goltz syndrome (SGG) is a rare autosomal dominant disorder. Although it is hereditary, there ...