Literature DB >> 8236968

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

C Cadrin1, M S Golbus.   

Abstract

Invasive prenatal testing has become an important way to evaluate fetuses at increased risk for hereditary disorders. In utero sampling of fetal skin, liver, and muscle may be required to diagnose before-birth disorders that cannot be diagnosed by analysis using chorionic villi or amniotic fluid. In the next few years, many of these conditions will be detected by DNA analysis, and the need for these procedures may decrease dramatically. First performed by fetoscopy, fetal tissue sampling is now most frequently done by inserting a biopsy needle under continuous ultrasonographic guidance. We describe the indications, techniques, complications, and experience with obtaining fetal skin, liver, and muscle biopsy specimens.

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Year:  1993        PMID: 8236968      PMCID: PMC1011339     

Source DB:  PubMed          Journal:  West J Med        ISSN: 0093-0415


  50 in total

1.  [Prenatal diagnosis of carbamyl phosphate synthetase deficiency by fetal liver biopsy].

Authors:  J Murotsuki; S Uehara; K Okamura; A Yajima; M Kikuchi; T Oura; S Miyabayashi
Journal:  Nihon Sanka Fujinka Gakkai Zasshi       Date:  1991-12

2.  Fetal liver biopsy for prenatal diagnosis of ornithine carbamyl transferase deficiency.

Authors:  C H Rodeck; A D Patrick; M E Pembrey; C Tzannatos; A E Whitfield
Journal:  Lancet       Date:  1982-08-07       Impact factor: 79.321

3.  Prenatal diagnosis of epidermolysis bullosa dystrophica Hallopeau-Siemens with electron microscopy of fetal skin.

Authors:  I Anton-Lamprecht; R Rauskolb; V Jovanovic; B Kern; M L Arnold; W Schenck
Journal:  Lancet       Date:  1981-11-14       Impact factor: 79.321

4.  Prenatal diagnosis of epidermolysis bullosa letalis.

Authors:  C H Rodeck; R A Eady; C M Gosden
Journal:  Lancet       Date:  1980-05-03       Impact factor: 79.321

5.  Prenatal diagnosis of genetic disorders of the skin by means of electron microscopy.

Authors:  I Anton-Lamprecht
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

6.  Prenatal diagnosis of hereditary skin disorders.

Authors:  S Elias; N B Esterly
Journal:  Clin Obstet Gynecol       Date:  1981-12       Impact factor: 2.190

7.  Cloning and sequence of a cDNA encoding human carbamyl phosphate synthetase I: molecular analysis of hyperammonemia.

Authors:  Y Haraguchi; T Uchino; M Takiguchi; F Endo; M Mori; I Matsuda
Journal:  Gene       Date:  1991-11-15       Impact factor: 3.688

8.  Prenatal diagnosis of harlequin ichthyosis.

Authors:  S Elias; M Mazur; R Sabbagha; N B Esterly; J L Simpson
Journal:  Clin Genet       Date:  1980-04       Impact factor: 4.438

9.  Prenatal diagnosis of congenital bullous ichthyosiform erythroderma (epidermolytic hyperkeratosis) by fetal skin biopsy.

Authors:  M S Golbus; R W Sagebiel; R A Filly; T D Gindhart; J G Hall
Journal:  N Engl J Med       Date:  1980-01-10       Impact factor: 91.245

10.  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

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  2 in total

1.  Metabolic Profile and Neurogenic Potential of Human Amniotic Fluid Stem Cells From Normal vs. Fetus-Affected Gestations.

Authors:  Giedrė Valiulienė; Aistė Zentelytė; Elizabet Beržanskytė; Rūta Navakauskienė
Journal:  Front Cell Dev Biol       Date:  2021-07-16

2.  Amniotic Fluid Stem Cells for the Treatment of Surgical Disorders in the Fetus and Neonate.

Authors:  Shaun M Kunisaki
Journal:  Stem Cells Transl Med       Date:  2018-08-07       Impact factor: 6.940

  2 in total

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