Congenital Hepatic Fibrosis and Autosomal Recessive Polycystic Kidney Disease in Children at Sohag University Hospital
Conditions
Brief summary
polycystic kidney disease is aherditary disorder characterized by the formation of numerous fluid filled cysts in the kidneys which can lead to progressive renal impairment PKDencompasses aspectrum of disorders with autosomal dominant polycystic kidneydisease and autosomal recessive polycystic kidney disease being the two main types
Interventions
OTHERabdominal ultrasound
abdominal ulterasound showing multiple cysts in the kidnets and hepatic fibrosis
Sponsors
Sohag University
Study design
Observational model
CASE_CROSSOVER
Time perspective
CROSS_SECTIONAL
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
* pediatric patients aged 0-18 years both male and female patients
Exclusion criteria
* patients whose guardians dont provide informed consent patients who are not complient with follow up vists and data collection protocols
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| incidence of congenital hepatic fibrosis in patient with autosomal recessive polycyctic kidney disease | 12 months | describe congenital hepatic fibrosis in patient with autosomal recessive polycystic kidney explaining their clinical manifestations.diagnosis.managment and complications |
Countries
Egypt
Outcome results
None listed