Araştırma Makalesi
BibTex RIS Kaynak Göster

A CASE WITH WOLFRAM (DIDMOAD) SYNDROME AND ORAL FINDINGS (A CASE REPORT)

Yıl 2007, Sayı: 014, 137 - 140, 17.12.2007

Öz

Wolfram Syndrome is an unusual, congenital, multi system disorder. Diabetes mellitus, Diabetes insipidus, optic

atrophy and deafness are most observable symptoms. Neurological, urinary tract and psychiatric disorders are the

other common symptoms. Diabetes mellitus and optic atrophy are usually the first findings.

In this case report we present 20 year old-male patient, that was have Wolfram syndrome. Oral clinical and

radiological findings were presented.

Kaynakça

  • [1] Internet: OMIM, In: Online Mendelian Inheritance in Man.http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?cmd=entry&id=222300 (2007)
  • [2] Swift, R.G., Sadler, D.B., Swift, M.,” Psychiatric findings in Wolfram syndrome homozygotes”, Lancet,336: 667-669 (1990).
  • [3] Barrett, T.G., Bundey, S.E., Macleod, A.F., “Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome”, Lancet, 2;346 (8988): 1458-63 (1995).
  • [4] Hardy, C., Khanim, F., Torres, R., Scott-Brown M., Seller A, Poulton J., Collier D., Kirk J.,Polymeropoulos M., Latif F., Barrett T., “Clinical and molecular genetic analysis of 19 Wolfram syndrome kindreds demonstrating a wide spectrum of mutations in WFS1”, Am J Hum Genet.,65(5):1279-90 (1999).
  • [5] Bu, X., Rotter, J.I., ”Wolfram syndrome: a mitochondrial-mediated disorder ?”, Lancet, 4;342 (8871):598-600 (1993).
  • [6] Sugano, N., Kawamoto, K., Numazaki, H., Murai, S., Ito, K., “Detection of mitochondrial DNA mutations in human gingival tissues”, J. Oral Sci., 42 (4):221-223 (2000).
  • [7] Zen, P.R., Pinto, L.L., Schwartz, I.V., Barrett, T.G., Paskulin, G., “Report of a Brazilian patient with Wolfram Syndrome”, J. Pediatr (Rio J)., 78(6): 529-32 (2002).
  • [8] Rotig, A., Cormier, V., Chatelain, P., Francois, R., Saudubray, J.M., Rustin, P., Munnich, A., ”Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy, and deafness (Wolfram syndrome, MIM 222300)”, J. Clin. Invest., 91(3): 1095-8 (1993).
  • [9] Langlais, R.P., Miller, C.S., ”Color Atlas of Common Oral Diseases”, Lea & Febiger, Philadelphia/London, 46-47 (1992).
  • [10] Mealey, B.,” Periodontal Medicine”, Rose, F.L., Mealey B.L., Genco, R..J., Cohen, W.D., B.C. Decker Inc., Toronto, 121-150 (1999).
  • [11] Terezhalmy, G. T., “Internal Medicine for Dentistry, 2 nd edition”, Kaye, D., Rose, L.F., The C.V.Mosby Company, St Louis, 1153-1154 (1990).

WOLFRAM (DIDMOAD) SENDROMU BULUNAN BİR OLGUDAKİ ORAL BULGULAR (OLGU BİLDİRİMİ)

Yıl 2007, Sayı: 014, 137 - 140, 17.12.2007

Öz

Wolfram Sendromu, nadir görülen konjenital, birçok sistemi etkileyebilen sendromdur. Diabetes mellitus,

diabetes insipidus, optik atrofi ve sağırlık ile karakterizedir. Hastalarda nörolojik rahatsızlıklar ile üriner sistem

rahatsızlıkları ve psikolojik rahatsızlıklar da izlenir. Diabetes mellitus ve optik atrofi ilk ortaya çıkan bulgulardır.

Bu olgu raporunda 20 yaşındaki Wolfram sendromlu erkek hastanın klinik ve radyografik ağız bulguları

sunulmaktadır.

Kaynakça

  • [1] Internet: OMIM, In: Online Mendelian Inheritance in Man.http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?cmd=entry&id=222300 (2007)
  • [2] Swift, R.G., Sadler, D.B., Swift, M.,” Psychiatric findings in Wolfram syndrome homozygotes”, Lancet,336: 667-669 (1990).
  • [3] Barrett, T.G., Bundey, S.E., Macleod, A.F., “Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome”, Lancet, 2;346 (8988): 1458-63 (1995).
  • [4] Hardy, C., Khanim, F., Torres, R., Scott-Brown M., Seller A, Poulton J., Collier D., Kirk J.,Polymeropoulos M., Latif F., Barrett T., “Clinical and molecular genetic analysis of 19 Wolfram syndrome kindreds demonstrating a wide spectrum of mutations in WFS1”, Am J Hum Genet.,65(5):1279-90 (1999).
  • [5] Bu, X., Rotter, J.I., ”Wolfram syndrome: a mitochondrial-mediated disorder ?”, Lancet, 4;342 (8871):598-600 (1993).
  • [6] Sugano, N., Kawamoto, K., Numazaki, H., Murai, S., Ito, K., “Detection of mitochondrial DNA mutations in human gingival tissues”, J. Oral Sci., 42 (4):221-223 (2000).
  • [7] Zen, P.R., Pinto, L.L., Schwartz, I.V., Barrett, T.G., Paskulin, G., “Report of a Brazilian patient with Wolfram Syndrome”, J. Pediatr (Rio J)., 78(6): 529-32 (2002).
  • [8] Rotig, A., Cormier, V., Chatelain, P., Francois, R., Saudubray, J.M., Rustin, P., Munnich, A., ”Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy, and deafness (Wolfram syndrome, MIM 222300)”, J. Clin. Invest., 91(3): 1095-8 (1993).
  • [9] Langlais, R.P., Miller, C.S., ”Color Atlas of Common Oral Diseases”, Lea & Febiger, Philadelphia/London, 46-47 (1992).
  • [10] Mealey, B.,” Periodontal Medicine”, Rose, F.L., Mealey B.L., Genco, R..J., Cohen, W.D., B.C. Decker Inc., Toronto, 121-150 (1999).
  • [11] Terezhalmy, G. T., “Internal Medicine for Dentistry, 2 nd edition”, Kaye, D., Rose, L.F., The C.V.Mosby Company, St Louis, 1153-1154 (1990).
Toplam 11 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Mühendislik
Bölüm Makaleler
Yazarlar

Hasan Hatipoğlu Bu kişi benim

Müjgan Güngör Hatipoğlu Bu kişi benim

Özden Kansu Bu kişi benim

Yayımlanma Tarihi 17 Aralık 2007
Yayımlandığı Sayı Yıl 2007 Sayı: 014

Kaynak Göster

APA Hatipoğlu, H., Hatipoğlu, M. G., & Kansu, Ö. (2007). A CASE WITH WOLFRAM (DIDMOAD) SYNDROME AND ORAL FINDINGS (A CASE REPORT). Journal of Science and Technology of Dumlupınar University(014), 137-140.