Prenatal diagnosis of a heterozygote of salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency by genetic linkage analysis.

For the purpose of prenatal diagnosis of CAH, genetic linkage analysis by HLA genotyping with lymphocytes and cultured amniotic cells were performed in a family at risk in which two consecutive children had been affected with SW CAH. In addition, the response of serum 17-OHP to intravenous ACTH was...

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Detalles Bibliográficos
Autores principales: Oh, B. H., Park, J. K., Choi, Y. M., Yang, I. M., Kim, Y. S., Choi, Y. K.
Formato: Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 1988
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3053666/
https://www.ncbi.nlm.nih.gov/pubmed/3267357

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