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Hereditary Sensory And Autonomic Neuropathy Type 1b C1842586

Published: July 22, 2026Updated: August 20, 2026

An inherited nerve disorder causing progressive loss of sensation and autonomic dysfunction, usually appearing in adolescence. Management includes preventing injuries and treating symptoms.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

Key facts at a glance

ICD-10
G43.909
ICD-11
8A00.0
Body system
neurologic
Severity
severe
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Generalized symptoms

(neurologic)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Sensory loss

(neurologic)

Foot ulceration

(neurologic)

Charcot arthropathy

(neurologic)

Orthostatic hypotension

(neurologic)

Diagnosis and tests

How this condition is diagnosed and what test results mean.

Initial screening tests

1

Standard diagnostic workup

Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]

Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]

Treatment options

Evidence-based approaches to managing this condition.

First-line treatments

1

Foot Care Protocol

Comprehensive daily foot inspection and care routine to prevent injuries and ulcers, including proper footwear selection and avoiding walking barefoot. Patient education on early wound recognition is essential.

lifestyle
2

Pharmacological management with first-line agents

Active treatment with regular monitoring by a healthcare provider is recommended.

medication
3

Gait Training and Balance Exercises

Therapeutic exercises to improve balance and proper gait patterns, reducing fall risk and preventing ankle injuries. May include use of assistive devices.

physical_therapy

Additional treatment options

Neuropathic Pain Management

Pharmacological approaches to manage burning or shooting pain associated with sensory neuropathy, typically using medications that target nerve pain pathways.

medication

Wound Care and Debridement

Surgical management of infected ulcers or tissue necrosis that fails conservative treatment, including debridement and possible amputation for non-healing wounds.

surgical

Regular Neurological Assessments

Periodic comprehensive neurological examinations to monitor sensory loss progression and autonomic function changes.

monitoring

When to seek medical help

Recognize when you need immediate medical attention.

See a doctor within 24 hours

Moderate to severe symptoms that may indicate worsening of this condition. Prompt medical evaluation is recommended.

Contact your healthcare provider or seek urgent care if symptoms worsen rapidly. Go to the emergency department for life-threatening symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Hereditary Sensory And Autonomic Neuropathy Type 1b C1842586?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Medication Comparisons

Compare medications used to treat Hereditary Sensory And Autonomic Neuropathy Type 1b C1842586. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy