Persistent Hypertransaminasemia Uncovered Occult Limb-Girdle-Muscle Dystrophy-Type-2C in a Saudi Child

• Main Authors: Naglaa M. Kamal (Author), Hamed A. Alghamdi (Author), Abdulrahman Halabi (Author), Abdullah O. Alharbi (Author), Muhammad Rafique (Author), Kamel Abidi (Author), Mortada H.H. El-Shabrawi (Author), Ayman E. Eskander (Author), Hala Mansour (Author), Laila M. Sherief (Author)
• 格式: 圖書
• 出版: Galenos Yayinevi, 2018-03-01T00:00:00Z.
• 主題: article
• 在線閱讀: Connect to this object online.

An asymptomatic 4.5 years-old Saudi girl was referred to the pediatric hepatology service with presumed liver disease because of the persistently elevated transaminases which were discovered accidently during routine laboratory workup. Alanine aminotransferase was 128 IU/L and aspartate aminotransfe...