Duchenne Muscular Dystrophy
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Delhi Court Notice To Centre On Request Of Boy Suffering From Rare Disease
The Delhi High Court today issued a notice to the Central Government on a plea moved by an 11-year-old child suffering from the rare disease Duchenne Muscular Dystrophy (DMD).
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"Why Were We Kept In Dark?": Delhi High Court On Rare Disease Clinical Trial
The Delhi High Court on Wednesday expressed its displeasure over being "kept in dark" about an ongoing trial here for Duchenne Muscular Dystrophy (DMD) when it has been dealing with issues pertaining to indigenous treatment of the rare disease.
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Court Expresses Displeasure Over No Treatment For Kids With Rare Disorder
The Delhi High Court on Tuesday expressed its displeasure over treatment not yet provided to the children suffering from the rare disease Duchenne muscular dystrophy (DMD) despite the direction of the court.
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Gene-Editing Technique Could Treat Muscular Dystrophy
A gene-editing technique has shown promise in treating Duchenne muscular dystrophy (DMD), the most common and severe form of muscular dystrophy among boys which is characterised by progressive muscle degeneration and weakness.
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World's First Blood Test for Accurate Prenatal Testing
Scientists at Plymouth University have developed a non-invasive, low risk and accurate blood test that can detect foetal blood group, sex, and genetic conditions in unborn babies.
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Indian-Origin Boy Denied Life-Saving Drug in UK
Six children, including a 6-year-old Indian-origin boy, has been denied life-saving treatment from a rare disease due to high costs by UK's state-funded health service.
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Muscular dystrophy affects mind too
Duchenne's muscular dystrophy (DMD) not only delays children's movement and coordination, but may also slow their language development.
-
Delhi Court Notice To Centre On Request Of Boy Suffering From Rare Disease
The Delhi High Court today issued a notice to the Central Government on a plea moved by an 11-year-old child suffering from the rare disease Duchenne Muscular Dystrophy (DMD).
-
"Why Were We Kept In Dark?": Delhi High Court On Rare Disease Clinical Trial
The Delhi High Court on Wednesday expressed its displeasure over being "kept in dark" about an ongoing trial here for Duchenne Muscular Dystrophy (DMD) when it has been dealing with issues pertaining to indigenous treatment of the rare disease.
-
Court Expresses Displeasure Over No Treatment For Kids With Rare Disorder
The Delhi High Court on Tuesday expressed its displeasure over treatment not yet provided to the children suffering from the rare disease Duchenne muscular dystrophy (DMD) despite the direction of the court.
-
Gene-Editing Technique Could Treat Muscular Dystrophy
A gene-editing technique has shown promise in treating Duchenne muscular dystrophy (DMD), the most common and severe form of muscular dystrophy among boys which is characterised by progressive muscle degeneration and weakness.
-
World's First Blood Test for Accurate Prenatal Testing
Scientists at Plymouth University have developed a non-invasive, low risk and accurate blood test that can detect foetal blood group, sex, and genetic conditions in unborn babies.
-
Indian-Origin Boy Denied Life-Saving Drug in UK
Six children, including a 6-year-old Indian-origin boy, has been denied life-saving treatment from a rare disease due to high costs by UK's state-funded health service.
-
Muscular dystrophy affects mind too
Duchenne's muscular dystrophy (DMD) not only delays children's movement and coordination, but may also slow their language development.
