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WGU D115 UNIT 2 EXAM QUESTIONS AND ANSWERS (LATEST UPDATE 2024) (46 QUESTIONS) VERIFIED.pdf

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WGU D115 UNIT 2 EXAM QUESTIONS AND ANSWERS (LATEST UPDATE 2024) (46 QUESTIONS) VERIFIED.pdf

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WGU D115 UNIT 2 EXAM QUESTIONS AND ANSWERS (LATEST UPDATE
2024) (46 QUESTIONS) VERIFIED


WGU D115 UNIT 2 EXAM QUESTIONS AND ANSWERS (LATEST UPDATE
2024) (46 QUESTIONS) VERIFIED


Which Type Of Genetic Disease Affects Males More Frequently Than Females?
Sex-Linked Recessive
Autosomal Recessive
Autosomal Dominant
Sex-Linked Dominant - Correct Answers ✅Sex-Linked Recessive. Since
Males Only Have One X And One Y, If The Affected Chromosome Has The
Illness, It Will Be Expressed.


In Which Two Conditions Are Chromosomal Abnormalities The Leading
Known Cause?


Intellectual Disability
Respiratory Disorders
Fetal Miscarriage
Cardiovascular Disease
Mental Illness
Check My Answer - Correct Answers ✅Intellectual Disability And Fetal
Miscarriage. Chromosome Abnormalities Are The Leading Known Cause Of
Intellectual Disability And Fetal Miscarriage.


What Are Three Examples Of Prenatal Diagnostic Studies?
Drug-Sensitivity Testing
Chorionic Villus Sampling (CVS)
Microscopy Of Cervical Mucosa



pg. 1

, WGU D115 UNIT 2 EXAM QUESTIONS AND ANSWERS (LATEST UPDATE
2024) (46 QUESTIONS) VERIFIED
Preimplantation Genetic Testing (PGT)
Amniocentesis - Correct Answers ✅Chorionic Villus Sampling (CVS),
Amniocentesis, And Preimplantation Genetic Testing (PGT) Are Examples Of
Prenatal Diagnostic Studies And Are Performed In Vitro. CVS Is A Form Of
Genetic Testing That Provides Genetic Information Found In Utero And Is
Usually Performed Between Weeks 11 And 14 Of Pregnancy. An Amniocentesis
Is A Form Of Genetic Testing That Evaluates Amniotic Fluid And Is Usually
Performed During The Second Trimester, Between Weeks 15 And 20 Of
Pregnancy. PGT Is Performed On The Embryo Prior To Implantation.


Which Genetic Disorder Is Characterized By The Presence Of A Zygote Having
One Chromosome With A Normal Complement Of Genes And One
Chromosome With A Missing Gene?
Klinefelter Syndrome
Down Syndrome
Cri Du Chat Syndrome
Turner Syndrome - Correct Answers ✅Cri Du Chat Syndrome (Translated As
"Cry Of The Cat") Is Caused By A DNA Deletion. This Term Describes The Cry
Often Heard From A Baby Affected By The Syndrome. Cri Du Chat Syndrome
Can Present As A Microcephalic, Low Birth-Weight Baby With A Piercing Cry.


How Can An X-Linked Recessive Disease Skip Generations?


Mothers Cannot Pass X-Linked Genes To Their Sons.
Females Are Hemizygous For The X Chromosome.
The Disease Can Be Transmitted Through Female Carriers.
These Diseases Need Only One Copy Of The Gene In Females. - Correct
Answers ✅The Disease Can Be Transmitted Through Female Carriers.


pg. 2

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