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What are the chances of a person with this disease passing the disease to their offspring (include possible scenarios)?
Scenarios:
Full Albino and Full Albino have a 100% chance of having an Albino child.
If both parents with albinism have the same type of albinism (i.e. OCA1, then the children will be affected), However if both parents have different types of albinism the children will be normally pigmented and carriers for both defective genes. (Leigh Lauflin)
Full Albino and Normal person have a 50% chance of an albino child and a 50% chance of a carrier, but normal child.
A heterozygous albino male and a carrier female have a 75% chance of getting an albino or carrier child and a 25% chance of getting a normal child.
This disease is found in 1 in 4 million people and the average life span is 13 years. It is autosomal dominate but due to a new mutation. If the person with the disease could even be even old enough to produce a child, the chances that the child would have the disease would be 100%.
Considering no one with Down's Syndrome would ever get laid, the chances are nil.
If you want the genetic stuff, look on Wikipedia.
Progeria is a very rare genetic disorder, affecting approximately 1 in 20 million births globally. Thus, the percentage of children with progeria is extremely low, less than 0.00001%.
Every 1 in 4 to 8 million children are born with Progeria or "Hutchinson Gilford Syndrome"
you cannot pass progeria on it is a chance occurance
It isn't a disease. It's a disorder. And the chances of a child being diagnosed with autism is
1 in 150 .
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Do black people get progeria?
Progeria is an extremely rare genetic condition that mainly affects children of all ethnicities. However, there have been reported cases of black children diagnosed with progeria, but it is still very uncommon.
Where can a punnett square for progeria be found?
A Punnett square is a tool used in genetics to predict the likelihood of certain traits being passed on from parents to offspring. Progeria is a rare genetic disorder characterized by accelerated aging in children. A Punnett square for progeria would not be relevant as it is not a trait that follows typical Mendelian inheritance patterns.
What is the chromosomal locus of progeria?
Progeria is caused by a mutation in the LMNA gene located on the long arm of chromosome 1 at position 1q22.
What is progreia?
Progeria is a rare genetic disorder that causes rapid aging in children. It is caused by a mutation in the LMNA gene, leading to symptoms such as growth retardation, hair loss, and cardiovascular problems. Unfortunately, individuals with progeria have a shortened lifespan, usually living only into their teens or early twenties.
What syndrome makes people grow old at a rapid pace?
Progeria is a genetic condition in which rapid signs of aging begin at a very young age. People with progeria usually do not live past 13 years of age.
Are people with progeria obese?
The exact opposite. Children with Progeria are extremely skinny.
Do black people get progeria?
Progeria is an extremely rare genetic condition that mainly affects children of all ethnicities. However, there have been reported cases of black children diagnosed with progeria, but it is still very uncommon.
Is progeria a dominant or recessive gene?
Progeria is caused by a dominant mutation in the LMNA gene. It is a rare genetic disorder that results in accelerated aging in children.
Is there a specific ethnic group or gender that is most likely to get progeria?
Progeria is commonly found in children of Asian/Polynesian decent.
Can adults get Progeria?
No, Progeria is a rare genetic condition that affects children, causing them to age rapidly. It is typically diagnosed in childhood and individuals with Progeria have a normal lifespan of around 13 years. It is not known to affect adults.
How many children die from progeria in one year?
1 out of2,500people
What is the name of the disease that causes rapid aging?
Progeria is the name of the disease that causes rapid aging in children. It is a rare genetic disorder that results in accelerated aging and affects various systems in the body.
Can kids with progeria have kids?
people with HGPS or progeria can have children although it is very unlikely to happen considering the fact that most only live to be 13 years old
What limitations do people with progeria have?
People with progeria have limitations such as growth retardation, early aging symptoms (wrinkled skin, hair loss), cardiovascular problems, joint stiffness, and reduced bone density. These limitations can impact mobility, physical development, and overall quality of life for individuals with progeria.
What individuals catch progeria?
Progeria is a rare genetic condition that occurs randomly, typically in children with no family history of the condition. It is caused by a mutation in the LMNA gene and cannot be passed down from parents.
Is progeria a recessive or dominant disorder?
Progeria is a dominant disorder caused by a mutation in the LMNA gene. It is characterized by accelerated aging in children.
Are there any Kids in Canada with Progeria?
The first cases I had become aware of with Progeria here in New Brunswick , Canada were 2 children ...brother and sister ....Ricky and Norma Gallant ...back in 1970.
