Accuracy of Non-Invasive Prenatal Testing for Duchenne Muscular Dystrophy in Families at Risk: A Systematic Review
Background: Methodological advancements, such as relative haplotype and relative mutation dosage analyses, have enabled non-invasive prenatal diagnosis of autosomal recessive and X-linked diseases. Duchenne muscular dystrophy (DMD) is an X-linked recessive disease characterized by progressive proxim...
Main Authors: | Luca Zaninović, Marko Bašković, Davor Ježek, Ana Katušić Bojanac |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2023-01-01
|
Series: | Diagnostics |
Subjects: | |
Online Access: | https://www.mdpi.com/2075-4418/13/2/183 |
Similar Items
-
Dystrophin and the two related genetic diseases, Duchenne and Becker muscular dystrophies
by: Elisabeth Le Rumeur
Published: (2015-07-01) -
Duchenne/Becker muscular dystrophy: A report on clinical, biochemical, and genetic study in Gujarat population, India
by: Mandava V Rao, et al.
Published: (2014-01-01) -
Duchenne muscular dystrophy treatment with lentiviral vector containing mini‐dystrophin gene in vivo
by: Xiaoyu Wang, et al.
Published: (2024-01-01) -
Language Delay in Duchenne’s Muscular Dystrophy
by: J Gordon Millichap
Published: (2007-06-01) -
Myelination is delayed during postnatal brain development in the mdx mouse model of Duchenne muscular dystrophy
by: Azeez Aranmolate, et al.
Published: (2017-08-01)