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What else can I help you with?
Is it possible for a woman to have muscular dystrophy?
Yep, both male and female can have it. I am a female and I have MD.
Why is pseudohypertrophic muscular dystrophy not to be expected in girls?
Pseudohypertrophic muscular dystrophy, commonly known as Duchenne muscular dystrophy (DMD), is primarily caused by mutations in the dystrophin gene located on the X chromosome. Since boys have only one X chromosome, they are more likely to express the disease when the gene is mutated. In contrast, girls have two X chromosomes, which means they would need mutations in both copies to exhibit the condition; this is much less common. As a result, girls are often carriers of the disorder rather than affected individuals.
When comparing Tay-Sachs disease and Duchenne's muscular dystrophy what disorders do they both have in common?
they both involve mutations in which fat replaces normal tissue
If the grandmother on the mothers side and the father of an unborn child both have Muscular Dystrophy what is the likelyhood of the child having it or being a carrier?
The likelihood of the child having Muscular Dystrophy (MD) or being a carrier depends on the specific type of MD and its inheritance pattern. If the mother's mother (grandmother) has an X-linked form of MD, there is a 50% chance that the child, if male, will be affected and a 50% chance that a female child will be a carrier. If the MD is autosomal recessive, then both parents would need to be carriers for the child to be affected, but the father, being male, may not be a carrier if he is affected. Genetic counseling is recommended for a more accurate assessment based on family history and genetic testing.
Can you donate plasma if you have muscular dystrophy?
In general, individuals with muscular dystrophy may be disqualified from donating plasma due to their medical condition, as it can affect muscle function and overall health. Plasma donation centers typically have specific health criteria that must be met, and conditions like muscular dystrophy may pose risks for both the donor and recipients. It's best to consult with the plasma donation center directly for their specific guidelines.
What are the most common diseases of the muscular system and what technologies that are used?
Two types of muscular diseases are muscle dystrophy and spinal muscle attrophy. Both are genetic, though.
A recessive gene located on the X chromosome is the cause of muscular dystrophy in affected individuals. Males are more likely to suffer from muscular dystrophy than females because?
males have only one X chromosome, so if they inherit the gene for muscular dystrophy on that X chromosome, they will develop the disorder. Females have two X chromosomes, so they would need to inherit the gene on both chromosomes to be affected, making it less likely for them to show symptoms.
If both parents are carriers what will the child be?
When a recessive trait is inherited from both parents, it will be expressed. If the trait is hemophilia, the child will be a hemophiliac.
How is duchene muscular dystrophy inherited?
Duchenne muscular dystrophy (DMD) is inherited in an X-linked recessive pattern, which primarily affects males. The condition is caused by mutations in the dystrophin gene located on the X chromosome. Since males have one X and one Y chromosome, a single mutated copy of the gene leads to the development of the disease. Females, having two X chromosomes, can be carriers if they have one mutated gene but typically do not show symptoms unless both X chromosomes carry the mutation.
What is same between als and muscular dystrophy?
Both amyotrophic lateral sclerosis (ALS) and muscular dystrophy are neuromuscular disorders that lead to progressive muscle weakness and atrophy. They both result from the degeneration of motor neurons or muscle fibers, affecting voluntary muscle control. Additionally, both conditions can significantly impact daily activities and quality of life for those affected. However, their underlying causes and specific symptoms differ.
How much shared DNA do two siblings typically have if their parents are both carriers of the gene for a hereditary condition?
Two siblings typically share about 50 of their DNA if their parents are both carriers of a gene for a hereditary condition.
How do you makelove to a man with muscular dystrophy in a wheelchair?
Making love to a man with muscular dystrophy in a wheelchair involves understanding and adapting to his physical needs and limitations. Communication is key; discuss preferences and comfort levels openly. Focus on intimacy through touch, kissing, and exploring different positions that work for both partners. Use supportive pillows or aids to enhance comfort and accessibility, ensuring a safe and pleasurable experience for both.
