Prenatal diagnosis of β-thalassemia

Haig H. Kazazian

Research output: Contribution to journalArticlepeer-review

2 Scopus citations


In this review I have discussed the state of our knowledge of the molecular basis of β-thalassemia and its prenatal diagnosis. Improved but more complicated genetic counselling is now available as a result of our increased knowledge of the effects of various defects in the β-globin gene. Our knowledge of the heterogenous molecular basis of the thalassemia syndromes has become very impressive and it is hoped that effective therapy will soon follow. However, for the present, prevention of the birth of affected children is the most effective means of reducing the suffering associated with the thalassemia syndromes, and prevention of this type is succeeding in many parts of the world, including North America.

Original languageEnglish (US)
Pages (from-to)15-24
Number of pages10
JournalSeminars in Perinatology
Issue number3 SUPPL. 2
StatePublished - Jun 1991

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Obstetrics and Gynecology


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