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Oral Medicine
Neurofibromatosis type 1 is an autosomal dominant disorder caused by a mutation in the NF1 gene, which produces neurofibromin. The gene is located on chromosome 17.
Prosthodontics
Examination of the patient revealed hyperplastic tuberosity touching the retromolar pad in the mandibular rest position. You would like to reduce the tuberosity before constructing complete dentures.
Physiology
The epithelial cells of the villi in the small intestine contain various digestive enzymes and microvilli that increase the surface area for nutrient absorption. These cells are crucial for the final stages of digesting carbohydrates and proteins,