Question

Fatty acid metabolism disorder is an autosomal recessive disorder. Two unaffected parents have 6 children -...

Fatty acid metabolism disorder is an autosomal recessive disorder. Two unaffected parents have 6 children - all of whom are unaffected.

List all of the mother's possible phenotypes.

Homework Answers

Answer #1

An autosomal recessive disease is inherited in an individual only under one condition. This condition is the presence of two copies lf the allele in the indiv. The individuals with a single copy are physiologically normal in nature since the disease does not pursue. However, they can transmit thus single allele to their offsprings.

According to the information, the unaffected parents have 6 unaffected children. Thus means that either all the children are not bearing the allele at all or they are all only carriers. The second condition can be possible only under the condition that either of the parents is a carrier.

Thus, the possible genotypes of the mother can be either As or aa.

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
Fatty acid metabolism disorder is an autosomal recessive disorder. Two unaffected parents have 6 children -...
Fatty acid metabolism disorder is an autosomal recessive disorder. Two unaffected parents have 6 children - 4 of whom are affected, and 2 of whom are unaffected. What are the chances that this couple will have a heterozygous child?
Gillespie syndrome (GS) is a rare genetic disorder. The disorder is characterized by having part of...
Gillespie syndrome (GS) is a rare genetic disorder. The disorder is characterized by having part of the iris missing, ataxia, and, in most cases, intellectual disability. It is termed as a heterogenous disorder because it can be inherited either through an autosomal dominant pattern or through an autosomal recessive pattern. Two parents are heterozygous for GS. A. Assuming that the condition is following an autosomal dominant pattern, what are the ratios or percentages of the genotypes AND phenotypes for the...
What is the probability that two parents, who are both carriers of an autosomal recessive disease,...
What is the probability that two parents, who are both carriers of an autosomal recessive disease, will have four children who are all affected by the disease? A) 25% B) 1.56 C) 0,39 D) 0
Two normal parents have a child with cystic fibrosis. Would this be an autosomal dominant or...
Two normal parents have a child with cystic fibrosis. Would this be an autosomal dominant or autosomal recessive disorder? What is the chance that their next child will have cyatic fibrosis?
Cystic fibrosis is an autosomal recessive disorder. Beth and Tom do not have cystic fibrosis but...
Cystic fibrosis is an autosomal recessive disorder. Beth and Tom do not have cystic fibrosis but each have a sibling with cystic fibrosis. Beth's parents and Tom's mother do not have the disease., but Tom's father does. Calculate the probability that if this couple has a child, the child will NOT have cystic fibrosis.
Albinism, a lack of pigmentation in humans, results from an autosomal recessive gene. Two parents with...
Albinism, a lack of pigmentation in humans, results from an autosomal recessive gene. Two parents with normal pigmentation have an albino child. What is the probability that their next two children will have the same genotype? a. 3/8 b. 11/16 c. 7/8 d. 13/16 e. 9/16
4. Two healthy parents have nine healthy children, but their tenth child exhibits severe mental and...
4. Two healthy parents have nine healthy children, but their tenth child exhibits severe mental and physical issues. What is the most likely cause?
 A. chromosomal inversion B. Autosomal Recessive disease C. Autosomal Dominant disease D. Chromosome 21 Non-disjunction E. All of the above
Sickle cell anemia is inherited as an autosomal, recessive disorder. Individuals who inherit the mutated gene...
Sickle cell anemia is inherited as an autosomal, recessive disorder. Individuals who inherit the mutated gene from both parents will show symptoms of sickle cell, including a stiffening of the red blood cells when the individual is under conditions with low oxygen levels in the air (e.g. on top of a mountain). This can lead to low red blood cell count (anemia), shortness of breath, fatigue, jaundice, and joint pain. Most critically, the stiffened red blood cells can clog small...
A widow’s peak is an autosomal dominant trait while a straight hairline is a recessive trait....
A widow’s peak is an autosomal dominant trait while a straight hairline is a recessive trait. Mike and his dad have a widow’s peak. Mike marries Bethany who has a continuous hairline like Mike’s mom. What is the probability that Mike and Bethany’s first child will have a widow’s peak? Complete Punnett Square to support your answer. Leave Blank Probability of first child: A 15-year old boy was diagnosed with a usual autosomal inherited form of diabetes. His mother was...
If two normal (disease free) parents each carry the recessive allele for cystic fibrosis, what is...
If two normal (disease free) parents each carry the recessive allele for cystic fibrosis, what is the chance one of their children could inherit the disease? Select one: 25% (1 out of 4) 100% (all children) 75% (3 out of 4) 50% (2 out of 4) No children Clear my choice If Woody Guthrie had children with a women with Huntingtons Disorder, which is true? Select one: no children would have it two out of four children having the disorder...