Sandbox:nou: Difference between revisions

Jump to navigation Jump to search
Line 13: Line 13:


==Pathophysiology==
==Pathophysiology==
The exact pathogenesis of Apraxia is not fully understood. It could be due to a defect in the brain pathways that comprise memory of learned forms of movement. Any disease that is related to these areas can lead to apraxia, stroke, dementia are the leading causes, but there are many other causes as well. The lesion cause could be because of certain metabolic, neurological, or other disorders that influence the brain, predominantly the frontal lobe, inferior parietal lobule of the left hemisphere of the brain. In this area, complex, 3-dimensional depictions of formerly learned patterns and movements are stored<ref>{{Cite web|url=https://rarediseases.org/rare-diseases/apraxia/#:~:text=Apraxia%20is%20caused%20by%20a,left%20hemisphere%20of%20the%20brain.|title=|last=|first=|date=|website=|archive-url=|archive-date=|dead-url=|access-date=}}</ref>. Patients with apraxia cannot regain these representations of stored, skilled actions.Therefore, patients with apraxia are unable to perform daily living activities well.
<br />


==Causes==
==Causes==

Revision as of 03:58, 22 June 2020

Dr Norina Usma

_NOTOC_


Historical Perspective

Classification

Based on whatever features apraxia is classified into

  • dadad
  • ffsf
  • fafa

Pathophysiology


Causes

Differentiating Xyz from Other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications, and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X-ray

There are no x-ray findings associated with apraxia.

Echocardiography and Ultrasound

CT scan

MRI

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Interventions

Surgery

Primary Prevention

Secondary Prevention

References