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Date May 2017 Marks available 2 Reference code 17M.2.SL.TZ2.3
Level Standard level Paper Paper 2 Time zone Time zone 2
Command term Outline Question number 3 Adapted from N/A

Question

Outline the use of human embryonic stem cells (hESC) to treat Stargardt’s disease.

[2]
a.

The most common form of Stargardt’s disease is known to be autosomal recessive. Using a Punnett grid, deduce the probability of a child inheriting Stargardt’s disease, if both of the parents are carriers of the disease but do not have the disease themselves.

[3]
b.

Markscheme

a. «an inherited form of» degeneration of retinal layer/photoreceptor cells/blindness 
OR
eye genetic disorder 

OWTTE

b. «hESC/stem cells» can provide/differentiate into healthy retinal cells 

c. injecting «hESC/stem cells» into the retina/eye can restore vision in animal/human trials

a.

a. correct allele identification 
«eg: S=dominant/normal; s=recessive/disease»

b. correct Punnett grid

c. correct phenotypic ratio/outcome

example:
s =recessive, disease-causing form of gene,
S =dominant,
normal form parents =Ss.
Any letter can be used as capital and lower case but a legend/key is not required if correct notation is used.

Do not award mp b if the gametes do not show heterozygous organisms

phenotypic ratio:
normal :  with disease
OR
3 normal : 1 with disease
OR
«75 % normal :» 25 % disease

b.

Examiners report

[N/A]
a.
[N/A]
b.

Syllabus sections

Core » Topic 1: Cell biology » 1.1 Introduction to cells
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Core » Topic 1: Cell biology
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