Atıf İçin Kopyala
Kavukcu S., DEMİR K., SOYLU A., Anal O., Saatci O., Goktay Y.
RHEUMATOLOGY INTERNATIONAL, cilt.25, sa.7, ss.555-557, 2005 (SCI-Expanded)
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Yayın Türü:
Makale / Tam Makale
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Cilt numarası:
25
Sayı:
7
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Basım Tarihi:
2005
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Doi Numarası:
10.1007/s00296-004-0557-7
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Dergi Adı:
RHEUMATOLOGY INTERNATIONAL
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Derginin Tarandığı İndeksler:
Science Citation Index Expanded (SCI-EXPANDED), Scopus
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Sayfa Sayıları:
ss.555-557
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Anahtar Kelimeler:
Alagille syndrome, Takayasu arteritis, VASCULAR ANOMALIES, ARTERITIS, MOYAMOYA
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Dokuz Eylül Üniversitesi Adresli:
Evet
Özet
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.