Wiedemann-Rautenstauch syndrome

Indian Pediatr. 2011 Sep;48(9):731-2.

Abstract

Wiedemann Rautenstauch (WR) syndrome is a rare autosomal recessive neonatal progeroid syndrome with only few published case reports. We describe a neonate showing clinical features of WR syndrome with peeling of skin, and presented with weak cry and breathing difficulty since birth.

Publication types

  • Case Reports

MeSH terms

  • Fatal Outcome
  • Female
  • Fetal Growth Retardation / diagnosis*
  • Fetal Growth Retardation / pathology
  • Fetal Growth Retardation / physiopathology
  • Humans
  • Infant, Newborn
  • Progeria / diagnosis*
  • Progeria / pathology
  • Progeria / physiopathology

Supplementary concepts

  • Progeroid syndrome, neonatal