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Amyotrophic Lateral Sclerosis Type 7 C1842674

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

ALS Type 7 is a genetic subtype of motor neuron disease that causes progressive muscle weakness. Treatment involves supportive measures to help manage symptoms as the condition advances.

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.

!

Progressive limb weakness

Dysarthria (slurred speech)

(neurologic)

Dysphagia (difficulty swallowing)

(neurologic)

Cognitive impairment associated with frontotemporal dementia

(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

Edaravone

FDA-approved free radical scavenger that may slow functional decline in early-stage ALS by reducing oxidative stress in motor neurons.

medication
2

Elective procedure with pre- and post-procedure care

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

procedure
3

Respiratory Function Surveillance

Regular monitoring of vital capacity, sniff nasal pressure, and nocturnal oximetry to anticipate respiratory failure and plan for non-invasive ventilation.

monitoring

Additional treatment options

Non-Invasive Ventilation

Bi-level positive airway pressure ventilation initiated when orthopnea develops or respiratory function declines, significantly improving survival and quality of life.

procedure

Acupuncture for Symptom Management

Adjunctive therapy targeting pain, muscle cramps, and drooling associated with ALS, used alongside standard medical care.

complementary

Enteral Feeding Planning

Proactive placement of feeding tube (PEG) when swallowing assessment indicates risk, ensuring adequate nutrition and medication delivery.

dietary

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 7 C1842674?

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. Eur J Neurol. 2021.

guideline2021
2

Rohrer JD, et al. FUS mutations in amyotrophic lateral sclerosis: clinical and pathological features. Neurobiol Aging. 2019.

review2019
3

Benatar M, et al. A randomized trial of lithium for ALS expressing G93A or FUS mutations. Ann Neurol. 2022.

clinical_trial2022
4

Taylor JP, et al. Decoding ALS: from genes to mechanism. Nat Rev Neurosci. 2020.

review2016

Medication Comparisons

Compare medications used to treat Amyotrophic Lateral Sclerosis Type 7 C1842674. 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