The Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies

Am J Med Genet. 1984 Sep;19(1):195-207. doi: 10.1002/ajmg.1320190120.

Abstract

We describe a familial syndrome of renal dysplasia, Wilms tumor, hyperplasia of the endocrine pancreas, fetal gigantism, multiple congenital anomalies and mental retardation. This condition was previously described by Perlman et al [1973, 1975] and we propose to call it the "Perlman syndrome." It appears to be transmitted as an autosomal recessive trait. The possible relationships between dysplasia, neoplasia and malformation are discussed.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / diagnosis*
  • Abnormalities, Multiple / genetics
  • Adult
  • Child
  • Child, Preschool
  • Female
  • Fetal Diseases / diagnosis*
  • Gigantism / diagnosis*
  • Humans
  • Intellectual Disability / diagnosis
  • Kidney / pathology
  • Kidney Neoplasms / diagnosis*
  • Kidney Neoplasms / pathology
  • Male
  • Pregnancy
  • Syndrome
  • Wilms Tumor / diagnosis*
  • Wilms Tumor / pathology