Variability of the Brachmann-de Lange syndrome

Am J Med Genet. 1993 Nov 15;47(7):977-82. doi: 10.1002/ajmg.1320470708.

Abstract

Brachmann-de Lange syndrome (BDLS) is a relatively common multiple congenital anomaly/mental retardation syndrome, whose cause is unknown. The clinical variability of this condition is well-known. Recently some reports suggested the possible existence of a mild BDLS phenotype. We report on 30 patients in whom a diagnosis of BDLS was made or strongly suspected in 12 different Italian hospitals. Based on clinical evaluation we divided them into two groups, classical and mild BDLS cases. We compare the clinical data of these patients and we discuss the problems which arise in trying to define clear criteria of distinction between these two groups.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • De Lange Syndrome / classification*
  • De Lange Syndrome / diagnosis
  • De Lange Syndrome / genetics
  • Face / abnormalities
  • Female
  • Growth Disorders / genetics
  • Humans
  • Infant
  • Infant, Newborn
  • Intellectual Disability / genetics
  • Limb Deformities, Congenital
  • Male
  • Phenotype
  • Psychomotor Disorders / genetics