Prenatal diagnosis of Smith-Magenis syndrome (del 17p11.2)

Dafydd G. Thomas, Suzanne M. Jacques, Leigh Anne Flore, Baruch Feldman, Mark I. Evans, Faisal Qureshi

Research output: Contribution to journalArticlepeer-review

20 Scopus citations

Abstract

Smith-Magenis syndrome is associated with a microdeletion of the short arm of chromosome 17 with phenotypic abnormalities including dysmorphic facies, self-injurious behavior, mental and neurologic disturbances, and congenital cardiac defects. The majority of patients present in mid-childhood or adulthood. We describe a fetus in which the diagnosis of Smith-Magenis syndrome was made at 16 weeks of gestation following amniocentesis for increased risk for Down syndrome detected by second-trimester maternal serum screening. Ultrasound evaluation revealed multiple fetal anomalies. The pregnancy was terminated at 20 weeks of gestation. Postmortem findings included dysmorphic facial features, tetralogy of Fallot, a thymic duct remnant, pancreatic islet cell hyperplasia, and abnormal lung fissuring. This represents the second case of prenatally diagnosed Smith-Magenis syndrome. Molecular genetic techniques in the diagnosis of the Smith-Magenis syndrome and other small deletions are becoming an important tool in the genetic evaluation of ultrasound abnormalities. Copyright (C) 2000 S. Karger AG, Basel.

Original languageEnglish
Pages (from-to)335-337
Number of pages3
JournalFetal Diagnosis and Therapy
Volume15
Issue number6
DOIs
StatePublished - 2000

Keywords

  • Chromosome 17
  • Microdeletion 17p11.2
  • Prenatal diagnosis
  • Smith-Magenis syndrome

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