Please confirm topic selection

Are you sure you want to trigger topic in your Anconeus AI algorithm?

Please confirm action

You are done for today with this topic.

Would you like to start learning session with this topic items scheduled for future?

Review Question - QID 101694

In scope icon M 2 D
QID 101694 (Type "101694" in App Search)
An 8-year-old boy is referred to your neurology clinic with the chief complaint of "trouble walking." His mother believes her son's condition has gradually worsened over the past several months with the recent development of difficulty coordinating his arms. Physical examination is notable for an ataxic gait, nystagmus, and mild dysarthria. You also observe the findings in Figure A on musculoskeletal examination. His mother believes that her husband's brother suffered from similar complaints and passed away at the age of 37 years. Which physical exam findings would you statistically most likely find in this patient's 3-year-old brother?
  • A

Systolic ejection murmur

11%

27/248

Telangiectasia

11%

27/248

Mental retardation

4%

11/248

Pes cavus

41%

101/248

Normal physical exam

29%

71/248

  • A

Select Answer to see Preferred Response

bookmode logo Review TC In New Tab

The constellation of ataxic gait, nystagmus, dysarthria, and pes cavus in a young adolescent is characteristic of Friedreich's ataxia. Friedreich's ataxia is an autosomal recessive disorder, with each child having a 25% chance of having clinical manifestations of the disease and a 75% chance of not having clinical disease. Thus, the patient's brother would most likely have a normal physical exam.

Friedreich's ataxia is an autosomal recessive trinucleotide repeat disorder (GAA) that leads to mutation of the frataxin gene. The frataxin gene is essential in mitochondrial iron regulation, and impairment of mitochondrial functioning results in cerebellar and spinal cord degeneration. Onset of Friedreich's ataxia is typically between 8-15 years of age, with gait ataxia being the usual presenting symptom. Physical exam may also reveal nystagmus, dysarthria, decreased vibratory and proprioceptive senses, and musculoskeletal findings such as kyphoscholiosis and pes cavus. Hypertrophic cardiomyopathy develops in more than 50% of patients, with cardiac arrhythmia and congestive heart failure as the cause of death in many patients with Friedreich ataxia.

Figure A depicts pes cavus, or a high arch of the foot that does not flatten with weight bearing. Friedreich's ataxia may cause muscle imbalances that leads to elevated arches.

Incorrect answers:
Answer 1. A systolic ejection murmur is characteristic of hypertrophic cardiomyopathy, a common cause of death in patients with Friedreich ataxia.
Answer 2. Telangiectasia may be seen in ataxia-telangiectasia, an autosomal recessive disorder characterized by progressive neurologic impairment, cerebellar ataxia, and ocular and cutaneous telangiectasia.
Answer 3. Mental retardation is a finding in many congenital disorders. The most common cause of inherited mental retardation is Fragile X syndrome, which results from a trinucleotide repeat expansion of CGG.
Answer 4. Pes cavus is a frequent physical finding in FA, which is characterized by a foot sole that is hollow when bearing weight, resembling a high arch.

Authors
Rating
Please Rate Question Quality

3.4

  • star icon star icon star icon
  • star icon star icon star icon
  • star icon star icon star icon
  • star icon star icon star icon
  • star icon star icon star icon

(23)

Attach Treatment Poll
Treatment poll is required to gain more useful feedback from members.
Please enter Question Text
Please enter at least 2 unique options
Please enter at least 2 unique options
Please enter at least 2 unique options