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Amyotrophic Lateral Sclerosis Type 6 C2931786

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

ALS Type 6 is an inherited progressive disorder damaging motor neurons that control movement. It affects both children and adults, and while there is no cure, care aims to maintain quality of life.

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

Key facts at a glance

ICD-10
G12.21
ICD-11
8A00.0
Body system
neurologic
Severity
fatal
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Warning signs - seek immediate care

!

Generalized symptoms

Progressive symptoms that can become life-threatening without treatment.

Seek immediate medical attention if symptoms worsen.

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Progressive muscle weakness

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Respiratory insufficiency requiring ventilatory support

Fasciculations (muscle twitching)

(neurologic)

Spasticity and hyperreflexia

(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

Image-guided procedure with follow-up care

Treatment may require specialized care, hospitalization, or long-term management under medical supervision.

procedure
2

Riluzole

FDA-approved glutamate antagonist that modestly extends survival in ALS patients by reducing excitotoxicity. Typically initiated at diagnosis and continued throughout disease course.

medication

Additional treatment options

Neuromuscular Physical Therapy

Specialized exercise program focusing on maintaining function, preventing contractures, and managing spasticity through gentle stretching and range-of-motion exercises.

physical_therapy

Nutritional Support and Caloric Management

Comprehensive nutritional assessment and intervention including high-calorie supplements and assisted feeding strategies as swallowing becomes impaired.

dietary

Psychological Support and Counseling

Individual and family counseling to address depression, anxiety, and adjustment to progressive disability, including grief support and coping strategies.

psychological

When to seek medical help

Recognize when you need immediate medical attention.

Call emergency services (911) immediately

!

Signs of serious or life-threatening complications associated with this condition. Immediate medical evaluation is required.

Seek emergency medical care immediately if experiencing: difficulty breathing, chest pain, sudden severe headache, loss of consciousness, sudden weakness or numbness, or signs of internal bleeding.

Frequently asked questions

Common questions about this topic.

Q

What is Amyotrophic Lateral Sclerosis Type 6 C2931786?

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

general

Sources and references

Authoritative medical sources used to create this content.

1

Andersen PM, et al. EFNS guidelines on the clinical management of amyotrophic lateral sclerosis (MALS): revised report of an EFNS task force. Eur J Neurol. 2021.

guideline2021
2

Renton AE, Chiò A, Traynor BJ. State of play in amyotrophic lateral sclerosis genetics. Nat Neurosci. 2014.

review2014
3

Miller RG, et al. Phase 3 trial of edaravone for amyotrophic lateral sclerosis. N Engl J Med. 2017.

clinical_trial2017
4

Taylor JP, Brown RH, Cleveland DW. Decoding ALS: from genes to mechanism. Nature. 2016.

review2016

Medication Comparisons

Compare medications used to treat Amyotrophic Lateral Sclerosis Type 6 C2931786. 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