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Incontinentia Pigmenti with Multiple Missing Teeth : Case Reports

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초록

Incontinentia pigmenti, also called Bloch-Sulzberger syndrome, is a rare X-linked inherited dominant disorder that affects females, but causes spontaneous abortion of prenatal males. Incontinentia pigmenti is a systemic disease with clinical features similar to ectodermal dysplasia, including congenitally missing teeth. The pathogenesis is related to gene mutations in NF-kappa-B essential modulator on chromosome Xq28. Incontinentia pigmenti is caused by a defect in the developmental stage of organs originating from the ectoderm or mesoderm and involves the skin, eyes, hair, teeth and central nervous system. This report discusses the management of three cases of 3 to 5 years old females with incontinentia pigmenti and accompanying multiple missing teeth. The cases had sparse hair, and showed oligodontia and anomalous crowns with supplementary cusps in the posterior teeth and conical anterior teeth. Removable space maintainers were applied, achieving improved esthetics, recovery of mastication and increased self-esteem in the patients.

Abstract

Incontinentia pigmenti, also called Bloch-Sulzberger syndrome, is a rare X-linked inherited dominant disorder that affects females, but causes spontaneous abortion of prenatal males. Incontinentia pigmenti is a systemic disease with clinical features similar to ectodermal dysplasia, including congenitally missing teeth. The pathogenesis is related to gene mutations in NF-kappa-B essential modulator on chromosome Xq28. Incontinentia pigmenti is caused by a defect in the developmental stage of organs originating from the ectoderm or mesoderm and involves the skin, eyes, hair, teeth and central nervous system. This report discusses the management of three cases of 3 to 5 years old females with incontinentia pigmenti and accompanying multiple missing teeth. The cases had sparse hair, and showed oligodontia and anomalous crowns with supplementary cusps in the posterior teeth and conical anterior teeth. Removable space maintainers were applied, achieving improved esthetics, recovery of mastication and increased self-esteem in the patients.

참고문헌 (25)

  1. Carney RG, "Incontinentia pigmenti : a world statistical analysis", Arch Dermatol, 112, pp.535~542 (1976)
  2. Phan TA, "Incontinentia pigmenti case series : clinical spectrum of incontinentia pigmenti in 53 female patients and their relatives", Clin Exp Dermatol, 30, pp.474~480 (2005)
  3. Wettke-Schafer R, "X-linked dominant inherited diseases with lethality in hemizygous males", Hum Genet, 64, pp.1~23 (1983)
  4. Gordon H, "Incontinentia pigmenti : clinical and genetical studies of two familial cases", Dermatologica, 140, pp.150~168 (1970)
  5. Curth HO, "The genetics of incontinentia pigmenti", Arch Dermatol, 92, pp.229~235 (1965)
  6. Takashi Y, "Case report :Orthodontic treatment of dental problems in incontinentia pigmenti", Angle Orthod, 68, pp.281~284 (1998)
  7. Wiklund DA, "Incontinentia pigmenti :A four-generation study", Arch Dermatol, 116, pp.701~703 (1980)
  8. Landy SJ, "Incontinentia pigmenti", J Med Genet, 30, pp.53~39 (1993)
  9. Niccoli-Filho WD, "Incontinentia pigmenti : a case report", J Clin Pediatr Dent, 17, pp.251~253 (1993)
  10. Domingues A, "General and dental characteristics of Bloch-Sulzberger syndrome : Reviews of literature and presentation of a case report", Med Oral, 7, pp.293~297 (2002)
  11. Russel DL, "Incontinentia pigmenti : a case report with emphasis on dental mianifestations", J Dent Children, 23, pp.206~208 (1956)
  12. Garrod AE, "Peculiar pigmentation of the skin of an infant", Trans Clin Soc Lond, 39, pp.216~ (1906)
  13. Curth HO, "The genetics of incontinentia pigmenti", Arch Dermatol, 92, pp.229~235 (1965)
  14. Smahi A, "Genomic rearrangement in NEMO impairs NF-KappaB activation and is a cause of incontinentia pigmenti", Nature, 405, pp.446~472 (2000)
  15. Berlin AL, "Incontinentia pigmenti : a review and update on the molecular basis of pathophysiology", J Am Acd Dermatol, 47, pp.169~187 (2002)
  16. Hadj-Rabia S, "Clinical study of 40 cases of incontinentia pigmenti", Arch Dermatol, 139, pp.1163~1170 (2003)
  17. 이상엽, "색소실소증 환아의 증례보고", 대한소아치과학회지, 32(4), pp.682~686 (2005), 대한소아치과학회
  18. Scott JG, "Ocular changes in the Bloch-Sulzberger Syndrome", Br J Ophalmol, 39, pp.276~282 (1955)
  19. Rosenfeld SI, "Ocular findings in incontinentia pigmenti", Ophthalmology, 92, pp.543~246 (1985)
  20. Goldenberg MF, "Retinal and other manifestations of incontinentia pigmenti", Ophtalmology, 100, pp.1645~1654 (1993)
  21. Mangano S, "Incontinentia pigmenti :Clinical and neuroradiological feature", Brain Dev, 15, pp.362~366 (1993)
  22. Abimelec P, "Late, painful, subungual hyperkeratosis in incontinentia pigmenti", J Am Acad Dermatol, 13, pp.913~918 (1985)
  23. 신혜성, "색소실조증 환아의 치험례", 대한소아치과학회지, 36(4), pp.563~567 (2009), 대한소아치과학회
  24. Cenk D, "Orthodontic and orthopedic treatment of a patient with incontinentia pigmenti", Angle Orthod, 73, pp.763~768 (2003)
  25. Yamashiro T, "Case report : orthodontic treatment of dental problems in incontinentia pigmenti", Angle Orthod, 3, pp.281~284 (1998)

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