0
What else can I help you with?
What is the most common known genetic cause of autism spectrum disorder?
The most common known genetic cause of autism spectrum disorder is mutations in the genes responsible for regulating brain development and function. These mutations can disrupt communication between brain cells and affect how the brain processes information, leading to the symptoms of autism.
What usually increases the appearance of a genetic disorder?
The appearance of a genetic disorder is usually increased by factors such as consanguineous (related) parents, inherited mutations from both parents, or environmental factors that trigger the expression of genetic mutations.
Why is autism considered a genetic disorder?
Autism is considered to be a genetic disorder because it is caused by a persons genes. It's linked to a number of individual genes and genetic mutations.
Relate genetic variation and mutations to each other?
mutations cause genetic variation, and vice-versa. If there is a genetic variation (or lack of one), then this can effect the severity of the mutation.
What are some of possible consequence of mutations?
DNA mutations can cause genetic disorders such as cancer, Diabetes, and Asthma.
How do genetic disorders occur in humans?
Genetic disorders can be caused by a mutation in one gene (monogenic disorder), by mutations in multiple genes (multifactorial inheritance disorder), by a combination of gene mutations and environmental factors, or by damage to chromosomes (changes in the number or structure of entire chromosomes.
What genetic mutations can cause?
A genetic mutation can cause a variation, which may be harmless, or may be harmful, depending on where on the DNA molecule it occurs.
What are the causes of genetic human disorders?
The causes of genetic disorders areThey can be inherited through Parents;Mutations may occur;A deletion may occur.These are the causes of a genetic disorder.
True or false changes of a few as one DNA base can cause a genetic disorder?
True. Changes in just one DNA base, known as point mutations, can lead to genetic disorders by altering the instructions for making proteins. These mutations may disrupt normal protein function, leading to disease.
Does frame shift mutation affect hemophilia?
Frame shift mutations that occur on the X chromosome and within the potion of code that controls the formation of clotting factors can cause hemophilia. Frame shift mutations are only one of many types of mutations that can cause the disorder. For hemophilia it's not so much the type of mutation but the location of the mutation within the genetic code.
What is the cause of a genetic disorder?
A mutation in the gene makeup of the organism.
How can mutations cause genetic mutations in spite of your body's DNA repair enzymes?
Mutagens cause a change in DNA and by this way they can produce mutant DNA repair enzymes.
