Congenital Hepatic Fibrosis and Autosomal Recessive Polycystic Kidney Disease in Children at Sohag University Hospital

Sohag University30 enrolled

Overview

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

Study Type

OBSERVATIONAL

Enrollment

Conditions

Congenital Hepatic Fibrosis and Autosomal Recessive Polycystic Kidney Disease in Children at Sohag University Hospital

Interventions

abdominal ultrasoundOTHER

abdominal ulterasound showing multiple cysts in the kidnets and hepatic fibrosis

Eligibility

Sex: ALL

Medical Language ↔ Plain English

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

Locations (1)

Sohag university Hospital

Sohag, Egypt

RECRUITING

Outcomes

Primary Outcomes

incidence of congenital hepatic fibrosis in patient with autosomal recessive polycyctic kidney disease

describe congenital hepatic fibrosis in patient with autosomal recessive polycystic kidney explaining their clinical manifestations.diagnosis.managment and complications

Time frame: 12 months

Data from ClinicalTrials.gov

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