Hereditary Gingival Fibromatosis (HGF) is an extremely rare oral health condition which affects gum tissue and can often lead to severe discomfort and leave those affected unable to eat. While the specific cause of this disorder remains a mystery, medical professionals have observed that HGF tends to repeatedly occur throughout new generations in families. Keep reading to learn about HGF and how it can be treated.

The Symptoms of Hereditary Gingival Fibromatosis?

The symptoms of HGF will usually be undetectable after birth and while the affected child has primary teeth; this disorder has a tendency to rapidly develop as permanent teeth erupt from the gum surface. People who are affected by HGF will notice their gums growing to become significantly larger than normal, often entirely covering their teeth, making their face appear swollen, and leaving them unable to chew solid food. If it is left untreated, HGF can lead to severe infections of the gum tissue, and tooth loss.

Treatments for Hereditary Gingival Fibromatosis

The main treatment for HGV will require surgery to remove the excessive gum tissue followed with a careful routine to heal the remaining gum tissue. Patients who receive the surgery will need to follow a very thorough oral hygiene routine and attend oral health screenings frequently to avoid the development of health complications.

Schedule an appointment at Briggs Family Dentistry if you suspect that your child is affected with Hereditary Gingival Fibromatosis.