Myotonic Dystrophy Type I (MT-I) is a type of muscular dystrophy that results in muscle weakness and wasting.
People with MT-I experience gradual muscle weakness, which can progress over time. This can cause difficulty moving, walking, climbing stairs, and participating in everyday activities.
What is Muscular Dystrophy?
A muscular dystrophy is a group of neuromuscular diseases that affect the muscles. Symptoms may include difficulty moving, breathing, and eating.
A muscular dystrophy is a group of neuromuscular diseases that affect the muscles. Symptoms may include difficulty moving, breathing
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What is Guillain Barre Syndrome?
If you have Guillain Barre syndrome, you may find yourself with a pronounced tremor that starts in your hands and spreads throughout your body.
What is Ataxia disorder?
Ataxia is a disorder that affects movement and coordination. Symptoms can vary, but generally include problems with movement and reduced mobility
Amyotrophic lateral sclerosis (ALS) is a progressive neurological disease that affects the nervous system. The disease is caused by the death of cells in the brain and spinal cord.
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What is a Cerebral aneurysm?
A cerebral aneurysm is a condition in which there is an abnormal expansion of the blood vessels on one side of the brain.
What is trisomy 13?
Trisomy 13 is a condition that occurs when a baby has three copies of chromosome 13 instead of the normal two.
Symptoms of Trisomy in Children?
Trisomy is a rare genetic disorder that affects the development of the baby’s brain and spine.
What is Trisomy 18?
Trisomy 18 is a rare genetic condition that affects the development of the baby’s brain and spine. It is caused by the presence of three copies of chromosome 18.
Treatments for Turner Syndrome?
There is no one treatment that works for all Turner Syndrome patients.
Symptoms of Turner Syndrome?
Turner Syndrome is a disorder of the X chromosome that affects about one in every 500 female births.
