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Neuromuscular Diseases: specialties

Diseases we treat

Some of the main diseases we treat include:

Duchenne muscular dystrophy

This is the most common muscular dystrophy in childhood. We are pioneers in clinical trials in Spain and we monitor more than 150 patients a year.

It is not covered by public health

Spinal muscular atrophy (SMA)

We treat and conduct leading national and European clinical trials on this disease. We monitor more than 100 patients a year with genetically confirmed diagnoses.

It is not covered by public health

Congenital muscular dystrophies

These manifest themselves in the first few months of life with progressive muscular weakness and other conditions. There are several types, for example, laminopathies and collagen VI deficiency.

It is not covered by public health

Congenital myopathies

There are several diseases in this group with wide-ranging patterns that are caused by a muscle development defect. We are leading a molecular study on these diseases.

It is not covered by public health

Congenital myasthenia

We are experts in identifying this type of neuromuscular transmission disorder. Accurate diagnosis enables us to offer more therapeutic options.

It is not covered by public health

Hereditary neuropathies (Charcot-Marie-Tooth)

We have diagnosed more than 200 patients suffering from various types of Charcot-Marie-Tooth disease. We carry out clinical and psychosocial monitoring.

It is not covered by public health

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