Birt-Hogg-Dub, syndrome (MIM #135150) is characterized by the development of benign skin tumours called fibrofolliculomas, pulmonary cysts that may lead to pneumothorax and a high risk of developing kidney cancer. BHD is caused by mutations affecting the highly conserved protein folliculin (FLCN), which probably has a role in intracellular transport. Most of the research effort directed towards BHD has focused on understanding how loss of FLCN causes kidney cancer. The cutaneous manifestations have received comparatively little attention. Although understandable, it is unfortunate, as the fibrofolliculomas are highly accessible and thus potentially are an excellent system for trying to understand the basic pathobiology of BHD. Also, patient...
Background: Birt-Hogg-Dubé syndrome (BHDS) is a rare autosomal dominant inherited syndrome caused by...
Birt-Hogg-Dubé syndrome (BHD) is an autosomal-dominant genodermatosis characterized by skin fibrofol...
Background/Aims Birt-Hogg-Dubé (BHD) syndrome is a rare autosomal dominant disorder that is characte...
Birt-Hogg-Dub, syndrome (MIM #135150) is characterized by the development of benign skin tumours cal...
Birt-Hogg-Dubé syndrome (MIM #135150) is characterized by the development of benign skin tumours cal...
Patients suffering from a rare genetic disease called Birt-Hogg-Dubé (BHD) syndrome are at increased...
Birt-Hogg-Dubé syndrome (BHD) is a rare inherited condition, which predisposes to the development of...
Patients suffering from a rare genetic disease called Birt-Hogg-Dubé (BHD) syndrome are at increased...
Birt-Hogg-Dubé syndrome (BHD) is an autosomal dominant condition characterised clinically by skin fi...
Most cancer occurs as a sporadic disease, in which gene mutations or genomics alterations that cause...
Birt-Hogg-Dubé (BHD) syndrome is a rare genetic disorder that can cause benign skin tumours, cysts i...
Birt-Hogg-Dubé (BHD) syndrome is an autosomal-dominantly inherited cancer syndrome characterized by ...
Birt–Hogg–Dubé syndrome (BHD) is an autosomal dominant inherited disorder characterised by fibrofoll...
A 43-year-old man presented with white to skin-colored shiny papules on the face and neck. In additi...
Background: Birt-Hogg-Dubé syndrome (BHDS) is a rare autosomal dominant inherited syndrome caused by...
Birt-Hogg-Dubé syndrome (BHD) is an autosomal-dominant genodermatosis characterized by skin fibrofol...
Background/Aims Birt-Hogg-Dubé (BHD) syndrome is a rare autosomal dominant disorder that is characte...
Birt-Hogg-Dub, syndrome (MIM #135150) is characterized by the development of benign skin tumours cal...
Birt-Hogg-Dubé syndrome (MIM #135150) is characterized by the development of benign skin tumours cal...
Patients suffering from a rare genetic disease called Birt-Hogg-Dubé (BHD) syndrome are at increased...
Birt-Hogg-Dubé syndrome (BHD) is a rare inherited condition, which predisposes to the development of...
Patients suffering from a rare genetic disease called Birt-Hogg-Dubé (BHD) syndrome are at increased...
Birt-Hogg-Dubé syndrome (BHD) is an autosomal dominant condition characterised clinically by skin fi...
Most cancer occurs as a sporadic disease, in which gene mutations or genomics alterations that cause...
Birt-Hogg-Dubé (BHD) syndrome is a rare genetic disorder that can cause benign skin tumours, cysts i...
Birt-Hogg-Dubé (BHD) syndrome is an autosomal-dominantly inherited cancer syndrome characterized by ...
Birt–Hogg–Dubé syndrome (BHD) is an autosomal dominant inherited disorder characterised by fibrofoll...
A 43-year-old man presented with white to skin-colored shiny papules on the face and neck. In additi...
Background: Birt-Hogg-Dubé syndrome (BHDS) is a rare autosomal dominant inherited syndrome caused by...
Birt-Hogg-Dubé syndrome (BHD) is an autosomal-dominant genodermatosis characterized by skin fibrofol...
Background/Aims Birt-Hogg-Dubé (BHD) syndrome is a rare autosomal dominant disorder that is characte...