Локализованная спинальная мышечная атрофия

Эта категория включает в себя группу заболеваний с разнообразной формой слабости и аутосомно-доминантным или Х-сцепленным рецессивным наследованием со специфическими генетическими профилями.

• Локализованная СМА - [спинальная мышечная атрофия]

• localised SMA - [spinal muscular atrophy]

• Localised spinal muscular atrophy
• localised SMA - [spinal muscular atrophy]
• Distal form of spinal muscular atrophy
• Distal hereditary motor neuropathy
• Distal HMN - [hereditary motor neuropathy]
• Distal hereditary motor neuropathy, autosomal dominant
• Distal spinal muscular atrophy, autosomal dominant
• Distal HMN - [hereditary motor neuropathy] autosomal dominant
• Autosomal dominant benign distal spinal muscular atrophy
• Autosomal dominant congenital benign spinal muscular atrophy
• Distal hereditary motor neuropathy type 1
• DHMN1 - [Distal hereditary motor neuropathy type 1]
• Distal hereditary motor neuropathy type 2
• DHMN2 - [Distal hereditary motor neuropathy type 2]
• Distal hereditary motor neuropathy type 5
• DHMN5 - [Distal hereditary motor neuropathy type 5]
• Distal hereditary motor neuropathy type 7
• DHMN7 - [Distal hereditary motor neuropathy type 7]
• Distal hereditary motor neuropathy, autosomal recessive
• Distal spinal muscular atrophy, autosomal recessive
• Distal HMN - [hereditary motor neuropathy] autosomal recessive
• Autosomal recessive lower motor neuron disease with childhood onset
• Autosomal recessive distal spinal muscular atrophy type 4
• dSMA4 - [Autosomal recessive distal spinal muscular atrophy type 4]
• Distal hereditary motor neuropathy type 3 and type 4
• dSMA3 and dSMA4 - [Distal hereditary motor neuropathy type 3 and type 4]
• Distal hereditary motor neuropathy, Jerash type
• Distal spinal muscular atrophy type 2
• Spinal muscular atrophy with respiratory distress
• Distal hereditary motor neuronopathy type 6
• Severe infantile axonal neuropathy with respiratory failure
• SMARD - [Spinal muscular atrophy with respiratory distress]
• Distal hereditary motor neuropathy, X-linked
• Distal HMN, X-linked
• Distal spinal muscular atrophy, X-linked
• Scapuloperoneal form of spinal muscular atrophy
• SPSMA - [Scapuloperoneal form of spinal muscular atrophy]
• Facioscapulohumeral form of spinal muscular atrophy
• FSHSMA - [Facioscapulohumeral form of spinal muscular atrophy]
• Facioscapulohumeral form of spinal muscular atrophy with sensory loss
• Davidenkow Disease
• Scapulohumeral form of spinal muscular atrophy
• Oculopharyngeal form of spinal muscular atrophy
• Ryukyu type of spinal muscular atrophy
• Bulbospinal muscular atrophy
• Kennedy Disease
• Spinal and bulbar muscular atrophy