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Amyotrophic Lateral Sclerosis Type 8 C1837728

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

ALS Type 8 is a rare inherited form of ALS where motor neurons gradually deteriorate. It primarily affects adults, and care focuses on symptom management and maintaining function.

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.

!

Orthopnea (difficulty breathing when lying down)

Muscle stiffness (rigidity)

(neurologic)

Cramping during activity

(neurologic)

Involuntary weight loss

(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

Minimally invasive procedural intervention

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

procedure
2

Symptomatic Spasticity Management

Use of muscle relaxants such as baclofen or tizanidine to manage spasticity and improve comfort, positioning, and functional ability.

medication
3

Sialorrhea Control

Anticholinergic medications to reduce excessive drooling, with alternatives including botulinum toxin injections for refractory cases.

medication

Additional treatment options

Assistive Technology Integration

Early implementation of communication aids, environmental controls, and mobility devices to maintain independence and quality of life.

lifestyle

Respiratory Muscle Training

Specific breathing exercises to maintain cough effectiveness and delay respiratory decline, adapted to patient's current functional level.

physical_therapy

Cognitive-Behavioral Therapy

Structured psychological intervention addressing anxiety, depression, and coping with progressive loss of function and communication.

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 8 C1837728?

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

Miller RG, Brown RH Jr, Barkhaus PE. Evidence-based guidelines for the management of ALS. Neurology. 2021.

guideline2021
2

Rothstein JD, Tsai G. Neurodegenerative motor neuron diseases: ALS and related disorders. Ann Neurol. 2022.

review2022
3

Cudkowicz ME, Shefner JM, Schoenfeld DA. A randomized trial of creatine monohydrate in ALS. JAMA Neurol. 2020.

clinical_trial2020
4

Turner MR, Hardiman O, Benatar M. Controversies and priorities in amyotrophic lateral sclerosis. Lancet Neurol. 2023.

meta_analysis2023

Medication Comparisons

Compare medications used to treat Amyotrophic Lateral Sclerosis Type 8 C1837728. 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