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Morgagni-Steawart-Morel syndrome: Case report

Cilt: 10 Sayı: 3 30 Eylül 2019
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Morgagni-Steawart-Morel syndrome: Case report

Öz

Hyperostosis frontalis interna (HOFI) is characterized by the benign growth of the inner plate of the frontal bone. It is most common in older women. Etiology is unknown. Morgagni-Stewart-Morel syndrome(MSM) is characterized by HOFI, obesity, hirsutism and mental illnesses but these associations are mostly based only on case reports. MSM syndrome is misunderstood and less reported pathology. The clinical presentation is not well defined andits finding is usually coincidental. The patient may present variable symptomatology. The idea that we should keep in mind is that HOFI representthe main pattern of MSM. Thus, it is highly importantto specify the presence and degree of HOFI in radiological reports.

Anahtar Kelimeler

Kaynakça

  1. 1.Attanasio F,Granziera S, Giantin V, Manzato E. Full Penetrance of Morgagni-Stewart-Morel Syndrome in a 75-Year-Old Woman: Case Report and Review of the Literature. J Clin Endocrinol Metab 2013; 98: 453-57.
  2. 2.Nallegowda M, Singh U, Khanna M, Yadav SL, Choudhary AR, ThakarA .Morgagni Stewart Morel syndrome-additional features. Neurol India 2005; 53: 117-19.
  3. 3. Smith S, Hemphill RE. Hyperostosis frontalis interna. J. Neurol. Neurosurg Psychiatr 1956; 19: 42-45. 4.Klein D, Rosatti P, Mach RS, Ferrier PE, Rauch S: Morgagni-Morel syndrome: an independent clinical and genetic entity, demonstrated in a family study covering 4 generations. Schweiz Arch Neurol Neurochir Psychiatr 1973;112: 239-50.
  4. 5. Ruhli FJ, Henneberg M. Are hyperostosis frontalis interna and leptin linked? A hypothetical approach about hormonal influence on human microevolution. Med Hypotheses. 2002; 58: 378-81.
  5. 6.Rosatti. Family affected by hyperostosis frontalis interna (Morgagni-Morel Syndrome) through 4 successive generations. J Genet Hum 1972; 20: 207-52.
  6. 7.Koller MF, Papassotiropoulos A, Henke K et al. Evidence of a genetic basis of Morgagni-Stewart-Morel syndrome. A case report of identical twins. Neurodegener Dis. 2005; 2: 56-60.
  7. 8. Hershkovitz I, Greenwald C, Rothschild BM, et al. Hyperostosis frontalis interna: an anthropological perspective. Am J Phys Anthropol 1999; 109: 303-25.

Ayrıntılar

Birincil Dil

İngilizce

Konular

Sağlık Kurumları Yönetimi

Bölüm

Olgu Sunumu

Yayımlanma Tarihi

30 Eylül 2019

Gönderilme Tarihi

15 Ağustos 2018

Kabul Tarihi

10 Kasım 2018

Yayımlandığı Sayı

Yıl 2019 Cilt: 10 Sayı: 3

Kaynak Göster

APA
Doğan, E., & Mouline, M. (2019). Morgagni-Steawart-Morel syndrome: Case report. Turkish Journal of Clinics and Laboratory, 10(3), 434-436. https://doi.org/10.18663/tjcl.453912
AMA
1.Doğan E, Mouline M. Morgagni-Steawart-Morel syndrome: Case report. TJCL. 2019;10(3):434-436. doi:10.18663/tjcl.453912
Chicago
Doğan, Emrah, ve Marwa Mouline. 2019. “Morgagni-Steawart-Morel syndrome: Case report”. Turkish Journal of Clinics and Laboratory 10 (3): 434-36. https://doi.org/10.18663/tjcl.453912.
EndNote
Doğan E, Mouline M (01 Eylül 2019) Morgagni-Steawart-Morel syndrome: Case report. Turkish Journal of Clinics and Laboratory 10 3 434–436.
IEEE
[1]E. Doğan ve M. Mouline, “Morgagni-Steawart-Morel syndrome: Case report”, TJCL, c. 10, sy 3, ss. 434–436, Eyl. 2019, doi: 10.18663/tjcl.453912.
ISNAD
Doğan, Emrah - Mouline, Marwa. “Morgagni-Steawart-Morel syndrome: Case report”. Turkish Journal of Clinics and Laboratory 10/3 (01 Eylül 2019): 434-436. https://doi.org/10.18663/tjcl.453912.
JAMA
1.Doğan E, Mouline M. Morgagni-Steawart-Morel syndrome: Case report. TJCL. 2019;10:434–436.
MLA
Doğan, Emrah, ve Marwa Mouline. “Morgagni-Steawart-Morel syndrome: Case report”. Turkish Journal of Clinics and Laboratory, c. 10, sy 3, Eylül 2019, ss. 434-6, doi:10.18663/tjcl.453912.
Vancouver
1.Emrah Doğan, Marwa Mouline. Morgagni-Steawart-Morel syndrome: Case report. TJCL. 01 Eylül 2019;10(3):434-6. doi:10.18663/tjcl.453912

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