Dilemmas of genetic counseling during prenatal diagnosis of Fabry disease
✍ Scribed by E. C. Molnár; J. Tanyi; E. Tóth-Pál; C. Papp
- Publisher
- Springer Vienna
- Year
- 1998
- Tongue
- English
- Weight
- 50 KB
- Volume
- 1
- Category
- Article
- ISSN
- 1434-1816
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
A prospective study of the reproductive plans of 185 genetic counseling clients a t risk for birth defects not diagnosable prenatally found, 6 months after counseling, 1) a small increase in the number of pregnancies initiated and planned, compared to pregnancies planned before counseling; 2) an inc
Fabry disease is an X-linked recessive inborn error of glycosphingolipid catabolism that results from the deficient activity of the lysosomal enzyme ␣-galactosidase A (␣-Gal A). A rapid, reliable, and universal linkage method was developed for molecular carrier detection and prenatal diagnosis. By d