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- Title
Expanding our understanding of fetal genetic diseases: the beginning of in utero precision medicine.
- Authors
Wapner, RJ
- Abstract
As genetic technologies evolve, our understanding of the causes of fetal structural anomalies and related fetal genetic diseases will expand. For example, osteogenesis imperfecta type 3, a severe debilitating skeletal disorder, may benefit from in utero mesenchymal stem cell treatment or lethal conditions such as alpha thalassaemia may benefit from second-trimester gene therapy.
- Subjects
FETAL diseases; INDIVIDUALIZED medicine; FETAL abnormalities; 22Q11 deletion syndrome; SPINAL muscular atrophy; MEDICAL specialties &; specialists
- Publication
BJOG: An International Journal of Obstetrics & Gynaecology, 2021, Vol 128, Issue 2, p430
- ISSN
1470-0328
- Publication type
Article
- DOI
10.1111/1471-0528.16541