What causes gingival hyperplasia?

Amlodipine Nifedipine phenytoin felodipine I-cell disease ethotoin nitrendipine sarcoidosis diltiazem verapamil ciclosporin Peripheral giant cell granuloma Robinow-Silverman-Smith syndrome Gangliosidosis GM1, type 1 Cross-McKusick-Breen syndrome Chromosome 8 recombinant syndrome Ramon syndrome Rutherfurd syndrome Systemic infantile hyalinosis Juvenile hyaline fibromatosis Jones syndrome Gangliosidosis GM3 Eruptive odontogenic cyst Hereditary gingival fibromatosis Dentigerous cyst Wegener granulomatosis amyloidosis Zimmerman-Laband syndrome Alpha-mannosidosis.

Ciclosporin Ciclosporin; cyclosporine; cyclosporin; or ciclosporin A, cyclosporine A, or cyclosporin A, the extremely powerful immunosuppressant drug widely used in organ transplantation to prevent rejection wikipedia Peripheral giant cell granuloma Peripheral giant cell granuloma, an oral pathologic condition that appears in the mouth as an overgrowth of tissue due to irritation or trauma wikipedia Robinow-Silverman-Smith syndrome Robinow-Silverman-Smith syndrome (a rare genetic disorder involving facial abnormalities, shortening of the forearms, small hands and feet, and genital defects) Gangliosidosis GM1, type 1 Gangliosidosis GM1, type 1, the cause and medical condition with Mesh code "D016537" and DiseasesDB code "34496" Cross-McKusick-Breen syndrome Cross-McKusick-Breen syndrome (a syndrome of gingival fibromatosis, pigmentation disorders, microphthalmia, and delayed psychomotor development) Chromosome 8 recombinant syndrome Chromosome 8 recombinant syndrome (recombinant chromosome 8 with developmental delay, minor facial anomalies, eye abnormalities, high frequency otitis media and hearing loss, congenital heart disease, and genitourinary anomalies) Ramon syndrome Ramon syndrome (a slowly progressive syndrome involving cherubism, maxillary fibrous dysplasia, gingival enlargement, radiolucent lesions of the jaws, seizures, delayed mental development, stunted growth, and other defects) Rutherfurd syndrome Rutherfurd syndrome (a mild form of gingival hypertrophy with corneal opacity and failure of tooth eruption) Systemic infantile hyalinosis Systemic infantile hyalinosis, the cause and medical condition with DiseasesDB code "33053" Juvenile hyaline fibromatosis Juvenile hyaline fibromatosis, the cause and medical condition with DiseasesDB code "33054" Jones syndrome Jones syndrome, the cause and medical concept with DiseasesDB code "34027" Gangliosidosis GM3 Gangliosidosis GM3 (a ganglioside biosynthesis disorder caused by (N-acetylneuraminyl)-galactosylglucosylceramide N-acetyl transferase (E. C) Eruptive odontogenic cyst Eruptive odontogenic cyst, the cause and medical concept with DiseasesDB code "31540" Hereditary gingival fibromatosis Hereditary gingival fibromatosis, the cause and medical concept with DiseasesDB code "30743" Dentigerous cyst Dentigerous cyst (most common follicular odontogenic cyst) Wegener granulomatosis Wegener granulomatosis (a multisystemic disease of a complex genetic background) amyloidosis Amyloidosis (any disease manifested by the pathogenic accumulation of amyloid in organs and tissues) Zimmerman-Laband syndrome Zimmermann-Laband syndrome (a syndrome of gingival fibromatosis, hepatosplenomegaly, and anomalies of the nose, bones, and nails, occasionally associated with mental retardation) wikipedia Alpha-mannosidosis Alpha-mannosidosis, an autosomal recessive metabolic disorder that causes mental and physical deterioration wikipedia.

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