The Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies. 1984

Am J Med Genet A. 2013 Nov;161A(11):2691-6. doi: 10.1002/ajmg.a.36316.

Abstract

The ensuing paper by Professor Giovanni Neri and colleagues was originally published in 1984, American Journal of Medical Genetics 19:195–207. The original article described a new family with a condition that the authors designated as the Perlman syndrome. This disorder, while uncommon, is an important multiple congenital anomaly and dysplasia syndrome; the causative gene was recently identified. This paper is a seminal work and is graciously republished by Wiley-Blackwell in the Special Festschrift issue honoring Professor Neri. 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.

Keywords: Perlman syndrome; Wiedemann-Beckwith syndrome; Wilms tumor; ambiguous genitalia; aniridia; fetal gigantism; hemihypertrophy; hyperplasia of endocrine pancreas; mental retardation; multiple congenital anomalies; nephroblastomatosis; renal dysplasia; trisomy 18.

Publication types

  • Biography
  • Classical Article
  • Historical Article

MeSH terms

  • Fetal Macrosomia / history*
  • History, 20th Century
  • Humans
  • Wilms Tumor / history*

Supplementary concepts

  • Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor