| Literature DB >> 1892202 |
M I Evans1, A Greb, L M Kunkel, A J Sacks, M P Johnson, C Boehm, H H Kazazian, E P Hoffman.
Abstract
Deoxyribonucleic acid techniques can be used to diagnose Duchenne muscular dystrophy prenatally in male fetuses that are at risk. Deoxyribonucleic acid-based prenatal diagnosis can be impossible when there is only one prior affected male and there is no identifiable deletion or alteration. We performed fetal muscle biopsy in utero in such a case and documented the presence of dystrophin, thereby confirming normality in a male fetus at risk. This first in utero experience adds fetal muscle biopsy to the available procedures for fetal tissue diagnosis.Entities:
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Year: 1991 PMID: 1892202 DOI: 10.1016/0002-9378(91)90318-l
Source DB: PubMed Journal: Am J Obstet Gynecol ISSN: 0002-9378 Impact factor: 8.661