Non Alcoholic Fatty Liver, Phenylketonurias
Conditions
Brief summary
phenylketonuria (commonly known as PKU) is an inherited disorder that increases the levels of a substance called phenylalanine in the blood. PKU is usually associated with many metabolic complication including non-alcoholic fatty liver
Detailed description
this study will include PKU children sufferers 9n=40) with non-alcoholic fatty liver to be randomly assigned to group I (n=20) that will perform walking program (online supervised free walking that will be applied daily for eight weeks) or group II (N=20) that will act as waitlisted children
Interventions
this Group I will include PKU children sufferers (n=20) with non-alcoholic fatty liver that will perform walking program (online supervised free walking that will be applied daily for eight weeks)
Sponsors
Study design
Eligibility
Inclusion criteria
* PKU children * obese children * fatty liver children (non-alcoholic fatty liver)
Exclusion criteria
* cardiac children * diabetic children * neurogenic disorders * respiratory and renal problems
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| alanine transamianse | it will be assessed after eight weeks | it is a serum liver enzyme |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| aspartate tranaminase | it will be assessed after eight weeks | it is a serum liver enzyme |
| Gamma-glutamyl Transferase | it will be assessed after eight weeks | it is a serum liver enzyme |
| alkaline phosphatase | it will be assessed after eight weeks | it is a serum liver enzyme |
| triglycerides | it will be assessed after eight weeks | it will be measured in the serum |
| body mass index | it will be assessed after eight weeks | it will be measured after emptying bladder |
Countries
Egypt