Conditions

Amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis is a progressive disease of the motor neurons, the nerve cells that carry movement commands from the brain to the muscles. Both the upper and the lower motor neurons degenerate, producing a combination of weakness and wasting with stiffness and brisk reflexes that is characteristic of the condition. Sensation, and usually thinking, are spared, though a minority develop frontotemporal changes.

Quick answer

Amyotrophic lateral sclerosis is a progressive disease of the motor neurons, the nerve cells that carry movement commands from the brain to the muscles. Both the upper and the lower motor neurons degenerate, producing a combination of weakness and wasting with stiffness and brisk reflexes that is characteristic of the condition. Sensation, and usually thinking, are spared, though a minority develop frontotemporal changes.

How it starts

Onset is usually focal and asymmetric, which is why it is so often mistaken for something local at first. It may be a weak hand that drops things or cannot manage buttons, a foot that catches on kerbs, or slurred speech and difficulty swallowing when the bulbar muscles are affected first. Muscle twitching, visible rippling under the skin and cramps are common. Weight loss and shortness of breath on lying flat come later and are important, because respiratory involvement drives the prognosis more than limb weakness does.

Why electrodiagnostic testing matters here

There is no single blood test for this diagnosis. It is made clinically and supported by EMG and nerve conduction studies, which demonstrate the loss of motor nerve supply to muscles across different regions of the body while sensory studies remain normal. That pattern is what separates it from the conditions that mimic it, several of which are treatable: multifocal motor neuropathy, cervical myelopathy, myasthenia gravis, inclusion body myositis. Both offices operate AANEM-accredited electrodiagnostic laboratories, and the neurologist who orders the study performs and interprets it. MRI and blood work are used to exclude the mimics; imaging is arranged elsewhere.

How it is managed

A small number of drugs are approved to slow progression, riluzole among them, and the list changes as trials report, so it should be checked against a current source rather than an article. Genetic testing matters for a minority, because a specific treatment exists for one inherited form and trial eligibility often depends on genetics. Everything else is about function and comfort: swallowing and nutrition, breathing support, communication aids, mobility equipment, spasticity, saliva management and cramps. There is no cure at present, and being told that early is more useful than discovering it after a year of searching.

Where care happens

Multidisciplinary ALS clinics, which bring neurology, pulmonology, nutrition, physical and occupational therapy, speech therapy and social work into one visit, are the recognised standard, and this practice is not one. What happens here is the diagnostic work, including the electrodiagnostic studies, and referral into that kind of programme, alongside general adult neurology follow-up. Being clear about that division is more useful to patients than implying a service that does not exist.

About this practice

Clinical Neurology Specialists has been physician-owned since 1998, when Leo Germin, M.D., FAANEM founded it. Five board-certified neurologists and four advanced practice providers see patients at the Las Vegas and Henderson offices, each with its own AANEM-accredited electrodiagnostic laboratory.

Clinical Neurology Specialists is an adult outpatient neurology practice for patients 18 and older. The practice performs no surgery and operates no imaging suite, infusion suite or interventional pain programme, and provides no emergency or inpatient care.

Emergency & crisis resources: Clinical Neurology Specialists is not an emergency service. For stroke symptoms, a seizure lasting more than five minutes or any medical emergency, call 911 or go to the nearest emergency room. For a mental health crisis, call or text 988 (Suicide & Crisis Lifeline).

Frequently asked

Questions about amyotrophic lateral sclerosis

Can twitching muscles mean ALS?
Twitching alone, without weakness or wasting, is extremely common and usually benign. The combination that matters is twitching together with progressive weakness or muscle loss, and that combination warrants examination rather than reassurance from a search engine.
How is it diagnosed?
By clinical examination showing both upper and lower motor neuron signs, supported by EMG and nerve conduction studies and by tests that exclude conditions which imitate it. There is no single confirmatory blood test.
Is there a cure?
No. There is currently no cure. A small number of approved drugs modestly slow progression, and a great deal can be done for breathing, swallowing, mobility and communication, which is where quality of life is actually decided.
Do you run an ALS clinic?
No. This practice performs the diagnostic evaluation, including electrodiagnostic studies, and refers to a multidisciplinary ALS programme for ongoing care. Neurology follow-up continues here where that is useful.
Is it inherited?
Most cases are not, but a minority run in families, and genetic testing is appropriate where there is a family history or where onset is unusually early, because it affects both treatment options and counselling for relatives.

Physician-reviewed. Reviewed by the physicians of Clinical Neurology Specialists — board-certified neurologists, AANEM-accredited electrodiagnostic laboratories, physician-owned since 1998. Reviewed 1 August 2026. This article is general education for adults 18 and older and is not a substitute for a consultation.

Next step

Speak to a board-certified neurologist

Adults 18 and older, at the Las Vegas and Henderson offices. Call 702-804-1212 or request an appointment online.