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Perlman syndrome

Congenital Malformations and Chromosomal Abnormalities

Perlman syndrome is a rare overgrowth syndrome, also known as nephroblastomatosis-fetal ascites-macrosomia-Wilms tumor syndrome. It is caused by autosomal recessive mutations in the DIS3L2 gene. The condition is characterized by macrocephaly, unusually large size at birth, enlarged kidneys, renal dysplasia, dysmorphic facial features and an increased risk of Wilms tumor, a childhood kidney cancer. Neonatal mortality is high among affected babies.

Facts
Classification
Body System
Urinary System 1
Communicable or Non-communicable
Non-Communicable 1
Causative Agent
Causative Agent (category)
Genetic / Hereditary 1
Sources
1. Perlman syndrome (Wikipedia)
  • Lead
    nephromegaly, renal dysplasia
  • Lead [causative-agent-category]
    caused by autosomal recessive mutations in the DIS3L2 gene
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