Chromosome 10qter deletion syndrome: a review and report of three new cases. Review uri icon

Overview

abstract

  • We report on three patients with terminal deletions of chromosome 10q and compare them to 15 previously reported patients. A similar facial appearance with a prominent beaked nose, large and/or malformed ears, and a pattern of major abnormalities including severe mental retardation, cardiac anomalies, and anogenital anomalies are reviewed. We feel the manifestations of del 10qter are sufficiently distinct to suggest this diagnosis on clinical examination.

publication date

  • March 1, 1989

Research

keywords

  • Abnormalities, Multiple
  • Chromosome Aberrations
  • Chromosome Deletion
  • Chromosome Disorders
  • Chromosomes, Human, Pair 10

Identity

Scopus Document Identifier

  • 0024373340

Digital Object Identifier (DOI)

  • 10.1002/ajmg.1320320319

PubMed ID

  • 2658586

Additional Document Info

volume

  • 32

issue

  • 3