Neuromuscular Conditions we Treat

Becker's Muscular Dystrophy

Becker's muscular dystrophy is a disorder that causes the muscles of the pelvis and legs to get gradually weaker over time. This can lead to a number of complications as the disease progresses. Learn More About Becker's Muscular Dystrophy Here

Charcot-Marie-Tooth Disease

Of the inherited nerve disorders, Charcot-Marie-Tooth syndrome is one of the most common. It impacts the peripheral nerves, which are the nerves outside the brain and spinal cord. It impacts 1 in every 2,500 people in the US and is named for the three doctors who discovered the disorder. Learn More About Charcot-Marie-Tooth Disease Here

Congenital Muscular Dystrophy

Congenital muscular dystrophy refers to a group of muscular dystrophies that are present at birth or shortly afterward. They involve muscle weakness, joint stiffness and other symptoms that impact a child’s ability to move, breathe and even learn. Learn More About Congenital Muscular Dystrophy Here

Congenital Myopathies

Myopathies are diseases that impact the muscles. A congenital myopathy is a muscle disease that is present at birth. They can take on many forms, but almost all of them include lack of muscle tone or muscle weakness. Learn More About Congenital Myopathies Here

Duchenne Muscular Dystrophy

Muscular dystrophy is a genetic condition characterized by progressive muscle weakness, difficulties with movement and other symptoms. Duchenne muscular dystrophy is known for getting worse much more. Learn More About Duchenne Muscular Dystrophy Here

Emery-Dreifuss Muscular Dystrophy

Emery-Dreifuss muscular dystrophy is a form of muscular dystrophy that causes problems with the skeletal muscles and the heart. The joints most commonly impacted by this form of muscular dystrophy include the elbows, ankles and neck. Almost all adults with Emery-Dreifuss muscular dystrophy develop heart problems. Learn More About Emery-Dreifuss Muscular Dystrophy Here

Facioscapulohumeral (FSH) Muscular Dystrophy

Facioscapulohumeral muscular dystrophy is a common muscular dystrophy which affects certain muscles of the body causing muscle weakness and wasting (atrophy). Learn More About Facioscapulohumeral (FSH) Muscular Dystrophy Here

Hereditary Neuropathy

Hereditary neuropathy is a medical term that refers to a group of different inherited medical conditions that cause progressive loss of function (and sensation) from abnormally working nerves that carry signals from the spinal cord to muscles. Learn More About Hereditary Neuropathy Here

Inflammatory Myopathies

Myopathies are diseases that impact the muscles. An inflammatory myopathy is a disease that is chronic and involves inflammation, muscle weakness and sometimes muscle pain. The four main types are polymyositis, dermatomyositis, inclusion body myositis and necrotizing autoimmune myopathy. Learn More About Inflammatory Myopathies Here

Limb-Girdle Muscular Dystrophy

Muscular dystrophy is a chronic disease that causes gradual weakness and loss of muscle over time. Learn More About Limb-Girdle Muscular Dystrophy Here

Mitochondrial Disease

Mitochondria are the special compartments within most body cells that are responsible for producing energy for life and organ function. If there’s a problem with how the mitochondria function, this can be a categorized as a mitochondrial disease. It’s a potentially serious, life-threatening problem. Learn More About Mitochondrial Disease Here

Myasthenia Gravis (MG)

MG in a rare chronic autoimmune disease in children of all ages, it is characterized by muscle weakness of varying degree in many different areas of the body, it commonly affects the eyes, mouth, throat, arms and legs. Learn More About Myasthenia Gravis (MG) Here

Neuromuscular Scoliosis

When the curvature is caused by problems related to the spinal cord, the brain or the muscles of the body, it can be classified as neuromuscular scoliosis. Learn More About Neuromuscular Scoliosis Here

Peripheral Neuropathy

The peripheral nerves are the vast network of nerves that transmits messages from the central nervous system to the rest of the body. When these nerves don’t function normally it is known as a peripheral neuropathy. Learn More About Peripheral Neuropathy Here

Peroneal Nerve Injury/Palsy

The peroneal nerve is an important nerve in the lower leg. It provides sensory input from the lateral aspect of the lower leg and the dorsum (top) of the foot. It also provides motor input to the muscles responsible for dorsiflexion (lifting the foot off of the ground) and eversion of the foot. When this nerve becomes injured, it can lead to sensation and movement problems, most commonly, a condition known as foot drop. Learn More About Peroneal Nerve Injury/Palsy Here


Neuropathy refers to damage that occurs to the nerves. When this damage occurs to nerves of the peripheral nervous system, or those outside of the brain and spinal cord, it is known as polyneuropathy. It can be either acute (short-lived) or chronic (long-lasting). Learn More About Polyneuropathy Here

Pompe Disease

When the body doesn’t have enough alpha-glucosidase enzyme, it can’t break down glycogen, a complex carbohydrate. This condition is known as Pompe disease. Learn More About Pompe Disease Here

Spinal Muscular Atrophy (SMA)

Spinal muscular atrophy is a rare degenerative disorder in which the nerve cells in the upper and lower parts of the spinal cord don’t function normally, resulting in muscle wasting and weakness. Learn More About Spinal Muscular Atrophy (SMA) Here

Ullrich Congenital Muscular Dystrophy

Ullrich congenital muscular dystrophy is a form of muscular dystrophy that causes joint stiffness and muscle weakness that gradually becomes worse over time. Learn More About Ullrich Congenital Muscular Dystrophy Here