A group of disorders characterized by a chronic motor and sensory nerve damage and resulting in muscle weakness and atrophy often associated with mild to moderate sensory loss, depressed tendon reflexes, and high-arched feet.
A group of genetic, congenital muscle diseases generally characterized by diminished muscle tone, progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, and delays in reaching motor milestones such as sitting or standing unassisted.
Congenital myasthenic syndrome
Hereditary conditions resulting from a genetic defect at the junction where the nerve stimulates muscle activity that result in muscle weakness.
Inherited muscular disorders present at birth, including central core disease, nemaline rod myopathy, and myotubular myopathy.
Duchenne is the most common childhood muscular dystophy and is usually caused by a gene disorder, which results in progressive muscle weakness.
An inherited form of muscular dystrophy that initially affects the skeletal muscles of the face, shoulders and upper arms. Skeletal muscle weakness usually develops in other areas of the body as well.
Friedreich's ataxia (FA)
A rare inherited disease that causes nervous system damage and movement problems. It usually begins in childhood and leads to impaired muscle coordination (ataxia) that worsens over time.
A group of muscle diseases that involve inflammation of the muscles or associated tissues, such as the blood vessels that supply the muscles, leading to destruction of muscle tissue, weakness and atrophy.
A progressive, inflammatory autoimmune condition characterized by nerve numbing, tingling, pain, progressive muscle weakness, loss of deep tendon reflexes, fatigue, and abnormal sensations.
Lambert-Eaton myasthenic syndrome
A rare autoimmune disease caused by immune system attacks on muscle tissue that leads to mobility issues and muscle weakness.
A chronic autoimmune neuromuscular disease characterized by varying degrees of weakness of the skeletal (voluntary) muscles of the body.
Myotonic muscular dystrophy
The most common form of muscular dystrophy in adults usually appears any time from early childhood to adulthood; characterized by prolonged spasm or stiffening of muscles after use.
Neuropathies associated with systemic diseases
A peripheral nerve condition resulting from a systemic disease, such as diabetes. May affect nerve sensation, movement, gland or organ function, and other aspects of health, depending on the type of nerve affected.
A genetic disease that affects the spinal cord and nerves, resulting in muscle wasting and weakness.An autosomal recessive disease, both both males and females are equally affected, and that two copies of the gene, one inherited from each parent, are necessary to have the condition.
These and many other conditions are treated by our neuromuscular disorders team. Please call 650-723-6469 to inquire about a condition not listed here.
Representatives from Stanford's Neuromuscular Clinic, Neurosciences Department, Rehabilitation, Integrative Medicine, and the new Neuroscience building construction crew all participated in the ALS Ice Bucket Challenge.
Clinical trials are research studies that evaluate a new medical approach, device, drug, or other treatment. As a Stanford Health Care patient, you may have access to the latest, advanced clinical trials.
Open trials refer to studies currently accepting participants. Closed trials are not currently enrolling, but may open in the future.
For your convenience, you may check in for all same-day appointments at the Stanford Neuroscience Health Center through a centralized, check-in desk near the front lobby. In addition to all outpatient services, you also can access onsite pre-surgery consultations at the center.
Appointments are available by physician referral only. Call us to reschedule an appointment or to schedule a follow-up appointment.
PREPARE FOR YOUR APPOINTMENT
Check in 20 minutes prior to your appointment.
Bring records or films (preferably on disc) that are relevant to the purpose of your appointment.
Bring a pen and notepad to take notes if needed.
The length of your first appointment may vary. Diagnostic appointments take one or more hours.
Returning patients or those with an existing diagnosis will see part or all of the multidisciplinary clinic team. These appointments last from one to three hours.
AFTER YOUR APPOINTMENT
To reorder a prescription, have your pharmacy call us directly with your prescription information.
Unfortunately, it is not possible for us to see all patients who are referred to us. We screen all referrals to select those who will benefit the most from a consultation. Also, most of our clinics have a significant waiting period for new consultations. Please provide as much clinical information as possible so our staff may triage the referral to the appropriate sub-specialty clinic.
We recognize that some patients may need consultation sooner than routine scheduling permits. Our doctors are happy to speak with you to facilitate urgent visits on a case-by-case basis.
Stanford Health Care provides comprehensive services to refer and track patients, as well as provides the latest information and news for physicians and office staff. For help with all referral needs and questions visit Referring Physicians.
HOW TO REFER
To refer a patient, call our New Patient Coordinator at 650-723-6469 or fax the following information to 650-320-9443:
Patient's name, birthdate, address, phone number, and other relevant data
Insurance carrier and any required authorization
Referring physician's name, address, and phone number
Referral letter or a description of the patient's medical history, diagnosis and reason for referral; include issues for us to address and any preference of neurologist or subspecialty clinic.
Our coordinator will schedule directly with the patient. Our staff will usually call the patient within two to three working days of receiving the referral.
Track your patients' progress and communicate with Stanford providers securely online.