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Question

Gower's sign is positive in:

The correct answer is
Duchenne's dystrophy

Gower's Sign Explained

Gower's sign is a clinical finding indicating significant weakness in the proximal muscles of the lower limbs, specifically the hip and thigh muscles.

It is observed when an individual, typically a child, rises from a supine position by using their hands to support themselves, progressively pushing off the ground and "walking" their hands up their legs to achieve an upright stance. This maneuver is necessary because the primary muscles responsible for standing (hip extensors and quadriceps) are too weak to perform the action directly.

Condition Associated with Gower's Sign

Duchenne's muscular dystrophy is characterized by progressive degeneration of muscles, particularly affecting the proximal muscles first. This severe proximal muscle weakness directly leads to a positive Gower's sign, as patients struggle to stand without using their hands for support.

Analysis of Other Options

  • Peroneal muscle atrophy primarily affects the muscles of the lower leg, not the proximal muscles of the hip and thigh, making Gower's sign atypical.
  • Friedreich ataxia is a neurological disorder causing ataxia and coordination problems; while it affects motor function, Gower's sign is not a characteristic symptom.
  • Cerebellar disease affects balance and coordination due to problems in the cerebellum. It does not typically manifest with the specific proximal muscle weakness measured by Gower's sign.

Therefore, Gower's sign is a key indicator of proximal lower limb muscle weakness, prominently seen in Duchenne's muscular dystrophy.

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Important Questions from Neuropathies

  1. Consider the following clinical features : 

    1. Hypomimia 

    2. Dysphonia 

    3. Festination gait 

    4. Cogwheel rigidity 

    Which of the features given above are generally present in Parkinsonism?

  2. Circuits between the basal ganglia and the motor cortex constitute the extra pyramidal system which controls muscle tone, body posture and the initiation of movement. Lesions of the extra pyramidal system present clinically with :
  3. Consider the following statements regarding Transient Global Amnesia (TGA): 

    1. TGA mainly affects middle aged persons who present with abrupt, discrete loss of anterograde memory lasting for few hours. 

    2. During the episode, the patients are unable to record new memories resulting in repetitive questioning. 

    3. Consciousness is impaired during the episode and the patient is unable to perform even simple motor functions. 

    4. After 4-6 hours, memory function and behaviour return to normal but the patient has complete and persistent amnesia for the duration of the episode. 

    Which of the statements given above are correct?

  4. Which of the following correctly describes the primary position of the right eye in right 3rd cranial nerve palsy?
  5. Which one of the following distinguishes axonal degeneration from segmental demyelination on electrophysiological studies?
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