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A case of Takayasu disease with findings of incomplete Alagille syndrome |
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| Authors: | Salih Kavukçu Korcan Demir Alper Soylu Özden Anal Osman Saatçi Yiğit Göktay |
| Affiliation: | (1) Department of Pediatrics, Medical Faculty, Dokuz Eylül University, Mithatpa!["scedil"]("/content/rvwv508gprp17te7/xlarge351.gif") a Cad. No. 665/4, Küçükyal!["imath"]("/content/rvwv508gprp17te7/xlarge305.gif") , 35280 Izmir, Turkey;(2) Department of Ophtalmology, Medical Faculty, Dokuz Eylül University, Mithatpaa Cad. No. 665/4, Küçükyal, 35280 Izmir, Turkey;(3) Department of Radiology, Medical Faculty, Dokuz Eylül University, Mithatpaa Cad. No. 665/4, Küçükyal, 35280 Izmir, Turkey |
| Abstract: | A 16-year-old girl being followed up for Takayasu arteritis for the last 3 years was also found to have Alagille syndrome upon findings of atypical facies, posterior embryotoxon, high-pitched voice, osteopenia and hypogonadism. This case might imply a possible relationship between Takayasu arteritis and Alagille syndrome. |
| Keywords: | Alagille syndrome Takayasu arteritis |
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