Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: June 16, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Differential Diagnosis for Dysautonomia

The following differential diagnosis is organized into categories to help guide the diagnostic process.

  • Single Most Likely Diagnosis

    • Postural Orthostatic Tachycardia Syndrome (POTS): This is often considered the most likely diagnosis for patients presenting with dysautonomia, characterized by a rapid heart rate and other symptoms that occur upon standing.
  • Other Likely Diagnoses

    • Autonomic Dysfunction associated with Diabetes: Diabetes can cause autonomic neuropathy, leading to dysautonomia symptoms such as orthostatic hypotension, gastrointestinal disturbances, and genitourinary symptoms.
    • Multiple System Atrophy (MSA): A neurodegenerative disorder that affects the autonomic nervous system, leading to symptoms like orthostatic hypotension, urinary incontinence, and tremors.
    • Autoimmune Autonomic Ganglionopathy: An autoimmune disorder that targets the autonomic ganglia, resulting in widespread autonomic dysfunction.
  • Do Not Miss Diagnoses

    • Myocardial Infarction or Cardiac Arrhythmias: Although less common, cardiac issues can present with symptoms similar to dysautonomia, such as palpitations or syncope, and are critical to diagnose promptly.
    • Pheochromocytoma: A rare tumor of the adrenal gland that can cause episodic hypertension, tachycardia, and other symptoms that might be mistaken for dysautonomia.
    • Neurodegenerative Diseases (e.g., Parkinson's Disease, Lewy Body Dementia): These conditions can have autonomic dysfunction as part of their clinical presentation and are crucial to identify due to their implications for management and prognosis.
  • Rare Diagnoses

    • Familial Dysautonomia (Riley-Day Syndrome): A rare genetic disorder that affects the development of the autonomic nervous system, leading to severe dysautonomia.
    • Pure Autonomic Failure: A rare condition characterized by progressive autonomic dysfunction without other neurodegenerative features.
    • Dopamine Beta-Hydroxylase Deficiency: A rare genetic disorder that affects the synthesis of norepinephrine, leading to severe orthostatic hypotension and other autonomic symptoms.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.