Neuromuscular Disorders: A clinical Approach
Part I: Asymmetric motor weakness
Motor Neuron Diseases [ALS]
Hirayama disease and other focal amyotrophies
Multifocal motor neuropathy
Acute motor axonal neuropathy
Facioscapulohumeral muscular dystrophy
Progressive muscular atrophy
Post-polio syndrome
Part II: Symmetric proximal weakness
Duchenne and Becker muscular dystrophies
Spinal Muscular atrophy [SMA]
Idiopathic Inflammatory myopathies
Limb Girdle muscular Dystrophies [LGMDs]
Congenital Myasthenic syndromes [CMS]
Congenital muscular dystrophies
Congenital myopathies
Emery Dreifuss Muscular dystrophy
Oculopharyngeal muscular dystrophy
Part III: Symmetric distal weakness
Myotonic dystrophies [DM]
Distal myopathies
Distal hereditary motor neuropathies
Brown Vieletto Van Laere Syndrome
Part IV: Fluctuating weakness
Myasthenia Gravis [MG]
Lambert Eaton Myasthenic Syndrome
Periodic paralysis
Part V: Exercise intolerance, muscle stiffness, cramps and contractures
Metabolic myopathies
Peripheral nerve hyperexcitability syndromes
Non dystrophic myotonias
Part VI: Asymmetric sensory motor weakness
Individual neuropathies
Vasculitic neuropathy
Multifocal acquired demyelinating sensory and motor neuropathy
Brachial plexopathies
Lumbosacral plexopathies
Compressive Radiculopathies
Leprosy
Hereditary neuropathy with pressure palsy
Part VII: Symmetric sensory motor weakness
Guillain-Barré syndrome
Charcot-Marie-Tooth disease[CMT]
Chronic Inflammatory Demyelinating Polyradiculoneuropathy
X-linked Charcot Marie Tooth disease
Other Hereditary neuropathies
1
Other hereditary neuropathies
2
Neuropathies secondary to systemic diseases
Porphyrias.-Part VIII: Predominant sensory syndromes
Sensory ganglionopathies
Distal Acquired Demyelinating Symmetric neuropathy
Paraproteinemic neuropathies
Miller Fisher Syndrome.