Type 1 Fucosidosis Is a Rare Human Disease -1-Fucosidase),and Is Inherited in an Autosomal Recessive Manner
Multiple Choice
Type 1 fucosidosis is a rare human disease.Patients cannot hydrolyze the disaccharide fucose,and as a result have severe neurological decline and die by age 6.The disease is due to a defect in the gene that encodes the lysosomal enzyme that breaks down fucose ( -1-fucosidase) ,and is inherited in an autosomal recessive manner.Which of the following statements is ACCURATE about Type1 fucosidosis?
A) Ff and ff individuals will have the disease
B) Ff individuals will have the disease,because anyone with the mutant allele will have the disease
C) Ff individuals make enough -1-fucosidase to break down fucose and do not exhibit the condition
D) Two carriers for Type I fucosidosis have no chance of having a normal child
E) Both Ff individuals will have the disease,because anyone with the mutant allele will have the disease AND two carriers for Type I fucosidosis have no chance of having a normal child
Correct Answer:

Verified
Correct Answer:
Verified
Q71: The color of petunia flower can be
Q72: Anury is the absence or abbreviation of
Q73: Incomplete dominance is when<br>A)the phenotypes of a
Q74: Nearsightedness is dominant to normal vision and
Q75: Hemophilia A is an X-linked recessive genetic
Q77: The law of independent assortment states that
Q78: A homologous pair of chromosomes at the
Q79: What features of meiosis allow for independent
Q80: Polydactyly is a dominant trait that results
Q81: An individual with an SRY gene is