Literature DB >> 1892202

In utero fetal muscle biopsy for the diagnosis of Duchenne muscular dystrophy.

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.

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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


  4 in total

Review 1.  Molecular biology of neurological diseases.

Authors:  W J Cumming
Journal:  Postgrad Med J       Date:  1992-04       Impact factor: 2.401

Review 2.  Fetal tissue sampling--indications, techniques, complications, and experience with sampling of fetal skin, liver, and muscle.

Authors:  C Cadrin; M S Golbus
Journal:  West J Med       Date:  1993-09

3.  Prenatal diagnosis of Duchenne muscular dystrophy by fetal muscle biopsy.

Authors:  J A Kuller; E P Hoffman; M H Fries; M S Golbus
Journal:  Hum Genet       Date:  1992 Sep-Oct       Impact factor: 4.132

4.  Multiplex PCR for rapid detection of exonal deletions in patients of duchenne muscular dystrophy.

Authors:  Ritu Singh; Madhulika Kabra
Journal:  Indian J Clin Biochem       Date:  2006-03
  4 in total

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