A) An extra toe on one foot
B) A laterally curved fifth finger
C) Complete absence of fingers and toes
D) Fusion of two fingers on the right hand
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Multiple Choice
A) The "gestalt"
B) The general feel and overall appearance of the patient
C) Specific dysmorphic features, such as the shape of the face and the position of the ears
D) All of the above
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Multiple Choice
A) Routine physical assessment relies on personal history, and genetic assessment relies on the recorded family history.
B) Genetic assessment requires only inspection, and routine physical assessment involves inspection, palpation, and auscultation.
C) Genetic assessment encompasses routine physical assessment and always adds the consideration of genetic causes for findings.
D) Routine physical assessment is performed by all health-care professionals, and genetic assessment is performed only by genetic professionals.
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Multiple Choice
A) Assess the phenotypes of first-degree relatives.
B) Count the number of minor anomalies present.
C) Use an atlas that includes globally diverse populations.
D) Determine whether an identified dysmorphic feature is a malformation or a deformation.
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Multiple Choice
A) Hypertelorism
B) Hypotelorism
C) Hyperoculoci
D) Hypo-oculoci
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Multiple Choice
A) An abnormal developmental process
B) An abnormal organization of cells
C) A mechanical process
D) The breakdown of an originally normal developmental process
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Multiple Choice
A) It is the rarest facial anomaly.
B) These features are not found in isolation.
C) The causes are both genetic and environmental.
D) CL without CP is a minor anomaly, and CL with CP is a major anomaly.
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Multiple Choice
A) Obtain a genetics referral as soon as possible.
B) Assess for the presence of any other dysmorphic features.
C) Document the finding in the medical record as the only action.
D) Gently explain to the parents that this finding is cause for concern.
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Multiple Choice
A) The earlobes are aligned with the highest point of the upper lip.
B) The earlobes are aligned with the highest point of the bottom lip.
C) The roots of the ears are aligned with the outer canthus of the eyes.
D) The roots of the ears are aligned an inch below the outer canthus of the eyes.
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Multiple Choice
A) Genomic imprinting
B) Decreased penetrance
C) Genetic heterogeneity
D) Variable expressivity
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Multiple Choice
A) The excessively long limbs have reduced bone density, increasing the risk for fractures.
B) The disorder is associated with weakened blood vessel walls that could rupture during strenuous activity.
C) The disorder is associated with glycogen storage deficiency, and the individual could become seriously hypoglycemic during strenuous activity.
D) Although people with Marfan syndrome are tall, they also have poor balance that impairs gross motor coordination, increasing the risk for injury.
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Multiple Choice
A) A unilateral clubfoot
B) A sealed (imperforate) anus
C) The absence of a thyroid gland
D) The presence of six toes on each foot
Correct Answer
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Multiple Choice
A) A syndrome
B) An association
C) A sequence
D) A dysplasia
Correct Answer
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Multiple Choice
A) A dysmorphology
B) A major anomaly
C) A minor anomaly
D) A disruption
Correct Answer
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Multiple Choice
A) It is an inherited normal variation of an anatomical feature.
B) All three family members should be referred to a geneticist for a formal evaluation.
C) The family is most likely descended from Neanderthal ancestors rather than from Cro-Magnon ancestors.
D) This physical anatomical malformation is a type of deformation caused by prenatal compression of soft skull areas.
Correct Answer
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Multiple Choice
A) Pleiotropic
B) Teratogenic
C) Carcinogenic
D) Geneticomimetic
Correct Answer
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Multiple Choice
A) "There is a 3% to 5% risk that your next child will be affected."
B) "Looking at your family history, I can tell that there is a 20% risk that your next child will be affected."
C) "Let's make an appointment with a genetic counselor who will help determine your next child's risk."
D) "You should have carrier testing to find out if your next child is at risk."
Correct Answer
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