Clinical features and molecular analysis of the α thalassemia/mental retardation sydromes. I. Cases due to deletions involving chromosome band 16p13.3

A. O.M. Wilkie, V. J. Buckle, P. C. Harris, J. Lamb, N. J. Barton, S. T. Reeders, R. H. Lindenbaum, R. D. Nicholls, M. Barrow, N. C. Bethlenfalvay, M. H. Hutz, J. L. Tolmie, D. J. Weatherall, D. R. Higgs

Research output: Contribution to journalArticle

112 Scopus citations

Abstract

We describe eight patients who have α thalassemia which cannot be accounted for the Mendelian inheritance of abnormal α globin genes. Apart from the hematologic abnormality, the other universal clinical finding is mild to moderate mental handicap; there is also a broad spectrum of associated dysmorphic features. Initial analysis of the α globin gene complex (which maps to chromosome band 16p13.3), demonstrated that the α thalassemia results from failure of the patient to inherit an α globin allele from one of the parents. Using a combined molecular and cytogenetic approach, we have extended this analysis to show that all of these patients have 16p deletions which are variable in extent but limited to the terminal band 16p13.3; in at least four cases the deletion results from unbalanced chromosome translocation, and hence aneuploidy of a second chromosome is also present. The relatively nonspecific clinical phenotype contrasts with the other currently known microdeletion syndromes; this may reflect ascertainment bias in the recognition of such syndromes. This work represents the first step in the characterization of a new microdeletion syndrome that is probably underdiagnosed at present.

Original languageEnglish (US)
Pages (from-to)1112-1126
Number of pages15
JournalAmerican journal of human genetics
Volume46
Issue number6
StatePublished - Jun 12 1990

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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    Wilkie, A. O. M., Buckle, V. J., Harris, P. C., Lamb, J., Barton, N. J., Reeders, S. T., Lindenbaum, R. H., Nicholls, R. D., Barrow, M., Bethlenfalvay, N. C., Hutz, M. H., Tolmie, J. L., Weatherall, D. J., & Higgs, D. R. (1990). Clinical features and molecular analysis of the α thalassemia/mental retardation sydromes. I. Cases due to deletions involving chromosome band 16p13.3. American journal of human genetics, 46(6), 1112-1126.