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females
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Who does a male inherit an autosomal recessive disorder from?
A male can inherit an autosomal recessive disorder from both of his carrier parents, who each pass down a copy of the mutated gene. This results in the male having two copies of the mutated gene, leading to the manifestation of the disorder.
Is it true that a female with one copy of the allele will be a carrier and have the disorder?
It depends on the type of disorder being discussed. For X-linked recessive disorders, a female with one copy of the mutated allele (being heterozygous) will typically be a carrier but not exhibit symptoms of the disorder. However, for autosomal dominant disorders, having one copy of the allele is sufficient for the individual to express the disorder. Therefore, the specifics of the allele and disorder in question are crucial for an accurate answer.
A person who has inherited the autosomal recessive disorder called?
A person who has inherited an autosomal recessive disorder will have two copies of the mutated gene, one from each parent. This results in the individual expressing the disorder. Symptoms can vary depending on the specific disorder.
How is carrier different from a person that has a disorder?
The carrier typically remains unaffected by the disorder.
What type of genetic test provides information about an asymptomatic persons risk for having a child with a specific autosomal recessive disorder in the future?
Carrier screening is the type of genetic test that provides information about an asymptomatic person's risk of having a child with a specific autosomal recessive disorder. This test identifies whether an individual carries a mutated gene associated with the disorder, which is essential for assessing the risk of passing the condition to offspring. If both parents are carriers, there is a 25% chance with each pregnancy that their child will inherit the disorder.
Who does a male inherit an autosomal recessive disorder from?
A male can inherit an autosomal recessive disorder from both of his carrier parents, who each pass down a copy of the mutated gene. This results in the male having two copies of the mutated gene, leading to the manifestation of the disorder.
What are the chances of two parents who carry the gene for albinism an autosomal recessive disorder having a child without albinism?
If both parents carry the gene for albinism, which is an autosomal recessive disorder, there is a 25% chance their child will be affected by albinism, a 50% chance the child will be a carrier like the parents, and a 25% chance the child will neither have albinism nor be a carrier. Therefore, there is a 75% chance that their child will not have albinism, either being a carrier or completely unaffected.
Is suicidal behavior autosomal disorder?
well, technically, suicidal behavior can be triggered by almost anything. Autosomal disorders very rarely have anything to do with behavior. but, im confused by the way you worded your question. Is it ,"Is suicdal behavior an autosomal disorder?" or "Can suicidal behavior be caused by an autosomal disorder?"
Is huntington disease an autosomal disorder?
Yes. HD is a disease of autosomal dominant inheritance.
Is it true that a female with one copy of the allele will be a carrier and have the disorder?
It depends on the type of disorder being discussed. For X-linked recessive disorders, a female with one copy of the mutated allele (being heterozygous) will typically be a carrier but not exhibit symptoms of the disorder. However, for autosomal dominant disorders, having one copy of the allele is sufficient for the individual to express the disorder. Therefore, the specifics of the allele and disorder in question are crucial for an accurate answer.
Which of these is in autosomal recessive disorder?
You did not list a "these" to chose from.
Is cystic fibrosis a dominant or co-dominant disorder?
It is autosomal recessive and it is not a disorder! Cystic Fibrosis is a disease.
What type of genetic disease is Refsum?
Refsum disease is inherited as an autosomal recessive disorder, which means that two unaffected carrier parents have a 25% chance of having an affected child in every pregnancy.
A person who has inherited the autosomal recessive disorder called?
A person who has inherited an autosomal recessive disorder will have two copies of the mutated gene, one from each parent. This results in the individual expressing the disorder. Symptoms can vary depending on the specific disorder.
How is carrier different from a person that has a disorder?
The carrier typically remains unaffected by the disorder.
What category of genetic disorder is huntingtons disease?
Autosomal Dominant
Is alkaptonuria caused by a recessive or dominant allele?
Phenylketonuria is an autosomal recessive genetic disorder. The enzyme phenylalanine hydroxylase is necessary to metabolize phenylalanie, but when this enzyme doesnt work, phenylaline accumulates and is detected in the urine. The disease is detected during pregnancy, and if treated right away the newborn can develop normally. However, if left untreated, the brain will not develop properly.
