Restriction fragment length polymorphism study of families with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Taiwan.

J. S. Lee, H. M. Tsai, R. P. Shieh, S. H. Chen, W. Y. Tsai, Bon Chu Chung

Research output: Contribution to journalArticle

Abstract

Congenital adrenal hyperplasia (CAH) is a heterogeneous group of hereditary diseases characterized by deficient adrenal cortisol synthesis. Most CAH is due to 21-hydroxylase (C21) deficiency. Genomic DNA from several families with 21-hydroxylase deficiency and normal controls was analyzed by the Southern blot hybridization technique. The restriction fragment length polymorphism (RFLP) patterns using several endonucleases, such as Taq I, Eco RI and Pvu II, at the C21 gene locus showed a very low frequency of variability in normals and most of the patients with CAH. One proband with CAH lacked the characteristic 3.7 kb Taq I fragment probed with C21 cDNA. This may be due to gene conversion and/or deletion events in the functional C21 gene locus. On the other hand, genes closely linked to the C21 locus such as C4 and HLA-DR are highly polymorphic. Using these flanking genes as probes, it is easy to perform linkage analysis and identify the inheritance trait. Prenatal diagnosis will be possible in these affected families when an additional pregnancy is expected.

Original languageEnglish
Pages (from-to)534-540
Number of pages7
JournalJournal of the Formosan Medical Association = Taiwan yi zhi
Volume89
Issue number7
Publication statusPublished - Jan 1 1990

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Congenital Adrenal Hyperplasia
Taiwan
Restriction Fragment Length Polymorphisms
Genes
Deoxyribonuclease EcoRI
Gene Conversion
Inborn Genetic Diseases
Endonucleases
Gene Deletion
HLA-DR Antigens
Southern Blotting
Prenatal Diagnosis
Hydrocortisone
Complementary DNA
Pregnancy
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
DNA

All Science Journal Classification (ASJC) codes

  • Medicine(all)

Cite this

Restriction fragment length polymorphism study of families with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Taiwan. / Lee, J. S.; Tsai, H. M.; Shieh, R. P.; Chen, S. H.; Tsai, W. Y.; Chung, Bon Chu.

In: Journal of the Formosan Medical Association = Taiwan yi zhi, Vol. 89, No. 7, 01.01.1990, p. 534-540.

Research output: Contribution to journalArticle

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