Neuroscience and Spine Institute
1-800-924-7620
NEUROMUSCULAR
Neuroscience and Spine Institute has a unique strength in treating neuromuscular disorders including Amyotropic Lateral Sclerosis (ALS), also known as Lou Gehrig's disease, and is home to The Carolinas Neuromuscular/ALS-MDA Center, the Southeast's most comprehensive facility for the study and treatment of degenerative neuromuscular diseases. A multi-disciplinary team of specialists provides aggressive, proactive treatment plans, integrating research with patient care to find new solutions for the devastating neuromuscular disorders of ALS, multiple sclerosis, epilepsy and Parkinson's disease.
Carolinas Neuromuscular Program
The Carolinas Neuromuscular Program at Carolinas Medical Center is built around a model of comprehensive diagnostic and treatment services. The program supports specialty clinics dedicated to the treatment of a specific disease and general neuromuscular clinics serving both adult and pediatric patients. It also integrates the services of many subspecialists, each with a dedicated interest in treating neuromuscular disease. Constant improvements in diagnosis and treatment make such a comprehensive approach necessary.
The Staff
The staff of the Carolinas Neuromuscular Program includes multiple specialists,
most with formal training in neuromuscular disease. These specialists form a team
that regularly participates in all patient evaluations.
The practitioners in the group meet regularly to coordinate their efforts and discuss diagnostic and
treatment options. The staff maintains regular contact with referring physicians
and allied health personnel. Patients may be treated at Carolinas Medical Center
or in a facility closer to their homes.
The Services
Genetics
Advances in molecular biology have dramatically changed diagnostic
approaches to neuromuscular disease. The Carolinas Neuromuscular Program has
the ability to test for many genetic diseases using both commercially available
technology and by collaboration with other experimental laboratories. A genetic
counselor is available for education and counseling prior to testing and
following diagnosis.
Patient Education
The Carolinas Neuromuscular Program offers many forms of patient education. It
also maintains a close liaison with the Muscular Dystrophy Association, which
provides a large volume of patient education materials. In addition, the program
offers access to area support groups and national organizations for many disorders.
Biopsy
Muscle and nerve biopsies are periodically needed to assist in a neuromuscular
diagnosis. The Carolinas Neuromuscular Program and Carolinas Medical Center
maintain a comprehensive pathology laboratory for evaluating biopsy specimens.
They are also active in a national network of other leading neuromuscular centers
whose qualified experts collaborate on complex or unusual diagnoses.
Muscular Dystrophy Association
The Muscular Dystrophy Association
(MDA) sponsors clinics on a weekly basis.
These clinics take an interdisciplinary team approach toward initial diagnosis
and follow-up care for both children and adults. The MDA regularly refers
patients who might have a neuromuscular disease to the Carolinas Neuromuscular
Program for evaluation. The patient's primary care physician often collaborates
treatment efforts with the team after the evaluation. The MDA also provides assistance for
patients who need help financing the services and equipment necessary to maintain
an optimal quality of life.
Amyotrophic Lateral Sclerosis
The Carolinas ALS Center is part of the Carolinas Neuromuscular Program. Patients
who may have amyotrophic lateral sclerosis (ALS) are evaluated by the ALS study team
over a two-day period. At least 10 practitioners evaluate each patient in order to
obtain a base-line assessment. An integrated treatment plan is implemented at the
initial evaluation, often by providing the therapy and/or the equipment required.
The Team
The cooperation of many contributing specialists is an essential part of the
Carolinas Neuromuscular Program's comprehensive approach to diagnosing and
treating neuromuscular disease. Each of the specialists who regularly evaluate
patients has a commitment to and specialized training in neuromuscular
diseases. Total patient care is a high priority for the team members, and
regular meetings are held to facilitate communication among specialists.
Currently, the team includes members from the following specialties:
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Neurology |

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Pediatric neurology |

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Pulmonology |

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Orthopaedics |

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Gastroenterology |

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Nutrition |

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Physiatry |

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Neuromuscular pathology |

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Genetics |

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Respiratory therapy |

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Orthotics |

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Social work |

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Equipment specialists |

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Occupational therapy |

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Physical therapy |

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Neuromuscular nursing |
Patients seen in the ALS clinics benefit from an evaluation by all ALS team members
on every visit, they come every month.
Clinical Trials
Participation in national and local clinical trials is a high priority within the
Carolinas Neuromuscular Program. Patients are regularly made aware of research
opportunities for new trials exploring alternative medications as well as treatments.
The Clinics
A variety of specialty clinics are available to patients with specific problems:
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General Neuromuscular Clinic |

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MDA Clinic |

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Pediatric MDA Clinic |

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ALS Team Evaluation (new patients) |

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Multidisciplinary ALS Follow-up |

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Electrodiagnostic Laboratory |
To schedule a visit to a specialty clinic, call the Carolinas Neuromuscular Program at 704-446-6257 or 800-924-7620. Relevant patient records may be faxed to 704-446-6255.
Neuromuscular Diseases
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Muscular Dystrophies |

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Duchenne (pseudohypertropic) muscular dystrophy |

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Becker muscular dystrophy |

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Emery-Dreifuss muscular dystrophy |

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Limb-girdle muscular dystrophy |

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Facioscapulohumeral (Landouzy-Dejerine) muscular dystrophy |

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Myotonic dystrophy (Steinert's disease) |

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Oculopharyngeal muscular dystrophy |

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Distal muscular dystrophy |

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Congenital muscular dystrophy |
Motor Neuron Diseases:
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Amotrophic lateral sclerosis (ALS) |

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Infantile progressive spinal muscular atrophy (Type 1, Werdnig-Hoffman disease) |

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Intermediate spinal muscular atrophy (Type 2) |

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Juvenile spinal muscular atrophy (Type 3, Kugelberg-Welander disease) |

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Juvenile spinal muscular atrophy (Type 3, Kugelberg-Welander disease) |

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Adult spinal muscular atrophy (Aran-Duchenne type) |
Inflammatory Myopathies
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Polymyositis |

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Dermatomyositis |
Diseases of Neuromuscular Junction
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Myasthenia gravis |

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Lambert-Eaton (myasthenic) syndrome |
Diseases of Peripheral Nerves
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Charcot-Marie-Tooth disease (peroneal muscular atrophy) |

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Friedreich's ataxia |

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Dejerine-Soltas disease |
Metabolic Diseases of Muscle
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Phosphorylase deficiency (McArdle's disease) |

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Acid maltase deficiency (Pompe's disease) |

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Phophofructokinase deficiency (Tarui's disease) |

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Debrancher enyzme deficiency (Cori's or Forbes' disease) |

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Mitochondrial myopathy |

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Carnitine deficiency |

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Carnitine palmityl transferase deficiency |

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Phosphoglycerate kinase deficiency |

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Phosphoglycerate mutase deficiency |

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Lactate dehydrogenase deficiency |

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Myoadenylate deaminase deficiency |
Myopathies Due To Endocrine Abnormalities
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Hyperthyroid myopathy |

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Hypothyroid myopathy |
Other Myopathies
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Myotonia congenita |

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Paramyotonia congenita |

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Central core disease |

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Nemaline myopathy |

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Myotubular myopathy |

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Periodic paralysis |
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