Autosomal Recessive Polycystic Kidney

A genetic disorder with autosomal recessive inheritance, characterized by multiple CYSTS in both KIDNEYS and associated LIVER lesions. Serious manifestations are usually present at BIRTH with high PERINATAL MORTALITY.

Also Known As:

Polycystic Kidney Disease, Infantile, Type I; Polycystic Kidney, Autosomal Recessive; ARPKD; Polycystic Kidney Disease, Autosomal Recessive; Polycystic Kidney Disease, Infantile, Type 1; Polycystic Kidney and Hepatic Disease 1; Polycystic Kidney and Hepatic Disease 1 (Autosomal Recessive); Autosomal Recessive Polycystic Kidney Disease; Kidney, Polycystic, Autosomal Recessive

Urogenital Diseases: 126
- Urologic Diseases: 799
  - Kidney Diseases: 12250
    - Cystic Kidney Diseases: 461
      - Polycystic Kidney Diseases: 1968
        Autosomal Recessive Polycystic Kidney: 290
- Female Urogenital Diseases and Pregnancy Complications
  - Female Urogenital Diseases
    - Urologic Diseases: 799
      - Kidney Diseases: 12250
        Cystic Kidney Diseases: 461
        Polycystic Kidney Diseases: 1968
        Autosomal Recessive Polycystic Kidney: 290
- Male Urogenital Diseases
  - Urologic Diseases: 799
    - Kidney Diseases: 12250
      - Cystic Kidney Diseases: 461
        Polycystic Kidney Diseases: 1968
        Autosomal Recessive Polycystic Kidney: 290
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Multiple Abnormalities: 211
    - Polycystic Kidney Diseases: 1968
      - Autosomal Recessive Polycystic Kidney: 290
- Inborn Genetic Diseases: 11939
  - Ciliopathies: 604
    - Polycystic Kidney Diseases: 1968
      - Autosomal Recessive Polycystic Kidney: 290

Mohammed Shalabi Selected Research

Mohammed Shalabi Research Topics

Disease

Therapy/Procedure