Hereditary gingival fibromatosis

Hereditary gingival fibromatosis (HGF) is a rare genetic disorder characterized by the overgrowth of gingival tissue in the mouth. This condition is typically benign, but it can cause significant discomfort and aesthetic concerns for those affected.

Etiology

HGF is a genetic disorder, meaning it is caused by abnormalities in an individual's DNA. The condition is typically inherited in an autosomal dominant manner, meaning that an affected individual has a 50% chance of passing the disorder onto their offspring. However, cases of autosomal recessive inheritance have also been reported.

Several genes have been associated with HGF, including SOS1, SOS2, and GFAP. Mutations in these genes can disrupt normal cell signaling and lead to the overgrowth of gingival tissue.

Clinical Presentation

The primary symptom of HGF is the overgrowth of gingival tissue, which can cover part or all of the teeth. This can lead to difficulty eating and speaking, as well as aesthetic concerns. Other symptoms can include gingival inflammation, tooth displacement, and malocclusion.

Diagnosis

Diagnosis of HGF is typically based on clinical examination and family history. Genetic testing may also be used to confirm the diagnosis and identify the specific gene mutation causing the condition.

Treatment

Treatment for HGF typically involves surgical removal of the excess gingival tissue. This can improve the individual's ability to eat and speak, as well as their appearance. Regular dental hygiene is also important to prevent gingivitis and other oral health problems.

Prognosis

The prognosis for individuals with HGF is generally good. The condition is typically benign and does not affect overall life expectancy. However, individuals with HGF may require ongoing dental care and surgery to manage their symptoms.

See Also

• Gingival hyperplasia
• Genetic disorder
• Autosomal dominant
• Autosomal recessive

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