Coexisting Duchenne Muscular Dystrophy and Gilbert’s Syndrome: A Case Report
Gilbert’s syndrome is characterized by unconjugated hyperbilirubinemia. A 5-year-old boy presented to our hospital with mild hyperbilirubinemia. The patient had persistent unconjugated hyperbilirubinemia with high liver enzymes and creatine phosphokinase. Haemolysis was excluded by normal h...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Cukurova University
2013-08-01
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| Series: | Çukurova Üniversitesi Tıp Fakültesi Dergisi |
| Subjects: | |
| Online Access: | http://www.scopemed.org/fulltextpdf.php?mno=33694 |