Oral Mucosal Lesions

  • Vazken M. der Kaloustian
  • Amal K. Kurban

Keywords

Sponge Keratitis Hypospadias Neuroma Microcephaly 

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    McKusick, V.A.: Mendelian inheritance in man, 5th ed. Baltimore: Johns Hopkins University Press 1978Google Scholar
  2. 2.
    Gorlin, R.J, Červenka, J, Pruzansky, S.: Facial clefting and its syndromes. In: The clinical delineation of birth defects. Bergsma, D. (ed.), Vol. VII, No. 7, pt. XI, pp. 3–49. Baltimore: Williams & Wilkins Co. 1971Google Scholar
  3. 3.
    Červenka, J, Gorlin, R.J, Anderson, V.E.: The syndrome of pits of the lower lip and cleft lip and/or palate. Genetic considerations. Amer. J. hum. Genet. 19, 416–432 (1967)PubMedGoogle Scholar
  4. 4.
    Walker, J.C, Clodius, L.: The syndromes of cleft lip, cleft palate, and lobster-claw deformities of hands and feet. Plast. reconstr. Surg. 32, 627–636 (1963)PubMedCrossRefGoogle Scholar
  5. 5.
    Gorlin, R.J, Sedano, H.O, Červenka, J.: Popliteal pterygium syndrome. A syndrome comprising cleft lip-palate, popliteal and intercrural pterygia, digital and genital anomalies. Pediatrics 41, 503–509 (1968)PubMedGoogle Scholar
  6. 6.
    Rüdiger, R.A, Haase, W, Passarge, E.: Association of ectrodactyly, ectodermal dysplasia, and cleft lip-palate. The EEC syndrome. Amer. J. Dis. Child. 120, 160–163 (1970)PubMedGoogle Scholar
  7. 7.
    Pashayan, H.M, Pruzansky, S, Solomon, L.: The EEC syndrome. Report of six patients. In: The clinical delineation of birth defects. Bergsma, D. (ed.), Vol. X, No. 7, pp. 105–120. Baltimore: Williams & Wilkins Co. 1974Google Scholar
  8. 8.
    Thurston, E.O.: A case of median hare-lip associated with other malformations. Lancet 1909 II, 996–997CrossRefGoogle Scholar
  9. 9.
    Rischbieth, H.: Hare-lip and cleft palate. In: Treasury of human inheritance, Vol. I, pt. IV, Plate J. London: Cambridge University Press 1918Google Scholar
  10. 10.
    Curtis, E.J, Fraser, F.C, Warburton, D.: Congenital cleft lip and palate. Risk figures for counseling. Amer. J. Dis. Child. 102, 853–857 (1961)Google Scholar
  11. 11.
    Juberg, R.C, Hayward, J.R.: A new familial syndrome of oral, cranial, and digital anomalies. J. Pediat. 74, 755–762 (1969)PubMedCrossRefGoogle Scholar
  12. 12.
    Rosselli, D, Gulienetti, R.: Ectodermal dysplasia. Brit. J. plast. Surg. 14, 190–204 (1961)PubMedCrossRefGoogle Scholar
  13. 13.
    Roberts, J.B.: A child with double cleft of lip and palate, protrusion of the intermaxillary portion of the upper jaw and imperfect development of the bones of the four extremities. Ann. Surg. 70, 252 (1919)CrossRefGoogle Scholar
  14. 14.
    Gorlin, R.J, Anderson, V.E, Scott, C.R.: Hypertrophied frenuli, oligophrenia, familial trembling and anomalies of the hand. Report of four cases in one family and a forme fruste in another. New Engl. J. Med. 264, 486–489 (1961)PubMedCrossRefGoogle Scholar
  15. 1.
    Everett, F.G, Weskott, W.B.: Commissural lip pits. Oral Surg. 14, 202–209 (1961)CrossRefGoogle Scholar
  16. 2.
    Taylor, W. B, Lane, D. K.: Congenital fistulas of the lower lip. Associations with cleft lip-palate and anomalies of the extremities. Arch. Derm. 94, 421–424 (1966)PubMedCrossRefGoogle Scholar
  17. 1.
    Anderson, J, Cunliffe, W.J., Roberts, D.F., Close, H.: Hereditary gingival fibromatosis. Brit. med. J. 1969 III, 218–219CrossRefGoogle Scholar
  18. 2.
    Witkop, C.J,Jr.: Heterogeneity in gingival fibromatosis. In: The clinical delineation of birth defects. Bergsma, D. (ed.), Vol. VII, No. 7, pt. XI, pp. 210–221. Baltimore: Williams & Wilkins Co. 1971Google Scholar
  19. 3.
    Ramon, Y, Berman, W, Bubis, J.J.: Gingival fibromatosis combined with cherubism. Oral Surg. 24, 435–448 (1967)PubMedCrossRefGoogle Scholar
  20. 4.
    Laband, P.F, Habib, G, Humphreys, G.S.: Hereditary gingival fibromatosis. Report of an affected family with associated splenomegaly and skeletal and soft-tissue abnormalities. Oral Surg. 17, 339–351 (1964)PubMedCrossRefGoogle Scholar
  21. 1.
    Von Sallmann, L, Paton, D.: Hereditary benign intraepithelial dyskeratosis. I. Ocular manifestations. Arch. Ophthal. 63, 421–429 (1960)CrossRefGoogle Scholar
  22. 2.
    Witkop, C.J, Jr., Shankle, C.H, Graham, J.B, Murray, M.R, Rucknagel, D.L, Byerly, B.H.: Hereditary benign intraepithelial dyskeratosis. II. Oral manifestations and hereditary transmission. Arch. Path. 70, 696–711 (1960)PubMedGoogle Scholar
  23. 3.
    Witkop, C.J, Jr., Gorlin, R.J.: Four hereditary mucosal syndromes. Comparative histology and exfoliative cytology of Darier-White’s disease, hereditary benign intraepithelial dyskeratosis, white sponge nevus, and pachyonychia congenita. Arch. Derm. 84, 762–771 (1961)PubMedCrossRefGoogle Scholar
  24. 1.
    Melkersson, E.: Ett fall av recidiverande facialispares i samband med angioneurotiskt ödem. Hygiea 90, 737–741 (1928)Google Scholar
  25. 2.
    Rosenthal, C.: Klinisch-erbbiologischer Beitrag zur Konstitutionspathologie: Gemeinsames Auftreten von (rezidivierender familiärer) Facilislähmung, Angioneuroticischen Gesichtsödem und Lingua plicata in Arthritismus-Familien. Z. Neurol. Psychol. 131, 475–501 (1931)CrossRefGoogle Scholar
  26. 3.
    Kunstadter, R.H.: Melkersson’s syndrome. A case report of multiple recurrence of Bell’s palsy and episodic facial edema. Amer. J. Dis. Child. 110, 559–561 (1965)PubMedGoogle Scholar
  27. 4.
    Klaus, S.N, Brunsting, L.A.: Melkersson’s syndrome (persistent swelling of the face, recurrent facial paralysis, and lingua plicata): report of a case. Proc. Staff Mayo Clin. 34, 365–370 (1959)Google Scholar
  28. 1.
    Gorlin, R.J, Sedano, H.O, Vickers, R.A, Červenka, J.: Multiple mucosal neuromas, pheochromocytoma and medullary carcinoma of the thyroid — a syndrome. Cancer 22, 293–299 (1968)PubMedCrossRefGoogle Scholar
  29. 2.
    Schimke, R.N, Hartmann, W.H, Prout, T.E, Rimoin, D.L.: Syndrome of bilateral pheochromocytoma, medullary thyroid carcinoma and multiple neuromas. A possible regulatory defect in the differentiation of chromaffin tissue. New Engl. J. Med. 279, 1–7 (1968)Google Scholar
  30. 3.
    Walker, D.M.: Oral mucosal neuroma–medullary thyroid carcinoma syndrome. Brit. J. Derm. 88, 599–603 (1973)PubMedCrossRefGoogle Scholar
  31. 4.
    Ljungberg, O, Cederquist, E, von Studnitz, W.: Medullary thyroid carcinoma and phaeochromocytoma: a familial chromaffinomatosis. Brit. med. J. 1967 I, 279–281CrossRefGoogle Scholar
  32. 5.
    Cunliffe, W.J, Black, M.M, Hall, R., Johnston, I.D.A, Hudgson, P, Shuster, S, Gudmundsson, T.V, Joplin, G.F, Williams, E.D, Woodhouse, N.J.Y, Galante, L, Maclntyre, I.: A calcitonin-secreting thyroid carcinoma. Lancet 1968 II, 63–66CrossRefGoogle Scholar
  33. 1.
    Dawson, T. A.J, Pielou, W.D.: Geographical tongue in three generations. Brit. J. Derm. 79, 678–681 (1967)PubMedCrossRefGoogle Scholar
  34. 1.
    Halperin, V, Kolas, S, Jefferis, K, Huddleston, S, Robinson, H.B.G.: The occurrence of Fordyce spots, benign migratory glossitis, median rhomboid glossitis, and fissured tongue in 2,478 dental patients. Oral. Surg. 6, 1072–1077 (1953)PubMedCrossRefGoogle Scholar
  35. 2.
    Tobias, N.: Scrotal tongue and its inheritance. Arch. Derm. Syph. 52, 266 (1945)PubMedCrossRefGoogle Scholar
  36. 1.
    Kaplan, B.J.: The clinical tongue. Lancet 1961 I 1094–1097CrossRefGoogle Scholar
  37. 2.
    Koplon, B.S, Hurley, H.J.: Prominent pigmented papillae of the tongue. Arch. Derm. 95, 394–396 (1967)PubMedCrossRefGoogle Scholar
  38. 3.
    Norum, R.A.; Association of pigmented nails, pigmented fungiform papillae of tongue, and apocrine chromidrosis. In: The clinical delineation of birth defects. Bergsma, D. (ed.), Vol. X, No. 4, pt. XVI, pp. 351–352. Baltimore: Williams & Wilkins Co. 1974Google Scholar
  39. 4.
    Rao, D. C.: Tongue pigmentation in man. Hum. Heredity 20, 8–12 (1970)PubMedCrossRefGoogle Scholar
  40. 5.
    Rao, D. C.: Formal segregation analysis for tongue pigmentation in man. Hum. Heredity 23, 308–312 (1973)PubMedCrossRefGoogle Scholar
  41. 1.
    Cannon, A.B.: White sponge nevus of the mucosa (naevus spongiosus albus mucosae). Arch. Derm. Syph. 31, 365–370 (1935)CrossRefGoogle Scholar
  42. 2.
    Zegarelli, E.V, Everett, F.G, Kutscher, A.H, Gorman, J, Kupferberg, N.: Familial white folded dysplasia of the mucous membranes. Arch. Derm. 80, 59–65 (1959)CrossRefGoogle Scholar
  43. 3.
    Witkop, C.J, Jr., Gorlin, R.J.: Four hereditary mucosal syndromes. Comparative histology and exfoliative cytology of Darier-White’s disease, hereditary benign intraepithelial dyskeratosis, white sponge nevus, and pachyonychia congenita. Arch. Derm. 84, 762–771 (1961)PubMedCrossRefGoogle Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 1979

Authors and Affiliations

  • Vazken M. der Kaloustian
    • 1
  • Amal K. Kurban
    • 2
  1. 1.American University of Beirut and American University HospitalBeirutLebanon
  2. 2.Division of DermatologyAmerican University of Beirut and American University HospitalBeirutLebanon

Personalised recommendations