Renal Involvement in Various Pediatric Liver Diseases: Review of Literature and Report on Tyrosinemia Cases
Mona Mohammed Habeeb Allah;
Abstract
Background: Hereditary tyrosinemia type 1 (HT1) is an increasingly
recognized inborn error of metabolism among Egyptian children.
Aim: To define the presenting clinical, biochemical and imaging features,
the outcome of NTBC therapy and liver transplant
recognized inborn error of metabolism among Egyptian children.
Aim: To define the presenting clinical, biochemical and imaging features,
the outcome of NTBC therapy and liver transplant
Other data
| Title | Renal Involvement in Various Pediatric Liver Diseases: Review of Literature and Report on Tyrosinemia Cases | Other Titles | الإلإختلالال الكلوي في المرضي المصابين بأمراض الكبد المختلفة: رؤية تحليلية ودراسة حالالات التيروزينيميا | Authors | Mona Mohammed Habeeb Allah | Keywords | Renal Involvement in Various Pediatric Liver Diseases: Review of Literature and Report on Tyrosinemia Cases | Issue Date | 2010 | Description | Background: Hereditary tyrosinemia type 1 (HT1) is an increasingly recognized inborn error of metabolism among Egyptian children. Aim: To define the presenting clinical, biochemical and imaging features, the outcome of NTBC therapy and liver transplant |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| 95255r2600.pdf | 130.27 kB | Adobe PDF | View/Open |
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