Erschienen in:
01.09.2005 | Case Report
A case of Takayasu disease with findings of incomplete Alagille syndrome
verfasst von:
Salih Kavukçu, Korcan Demir, Alper Soylu, Özden Anal, Osman Saatçi, Yiğit Göktay
Erschienen in:
Rheumatology International
|
Ausgabe 7/2005
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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.