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Proximal Weakness: Difference between revisions
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{{family tree | | D01 | | D02 | | | | D03 | | |D01=<ul><li>[[Myositis|Inflammatory myositis]]<ul><li>Polymyositis</li><li>dermatomyositis</li><li>immune mediated necrotising myopathy </li></ul></li><li>Endocrine - e.g cushings, dysthyroid</li>Drugs<li>Hyper/hypokalaemia</li></ul>|D02=<ul><li>Becker's or Duchenne's muscular dystrophy</li><li>Limb girdle muscle dystrophies</li><li>Congenital myopathies </li><li>Mitochondrial</li><li>Metabolic ([[Glycogen Storage Diseases|glycogen or lipid disorder]])</li><li>[[Pompe Disease|Acid maltase]]</li></ul>|D03=<ul><li>Peripheral neuropathies with proximal weakness - vasculitis or [[Chronic Inflammatory Demyelinating Polyneuropathy|CIDP]]</li><li>Plexopathies e.g. [[Diabetic Amyotrophy|diabetic amyotrophy]]</li><li>Infiltration nerve root - neoplastic meningitis</li><li>[[Cervical Myelopathy|Myelopathy]]</li><li>Neuromuscular junction - Lambert Eaton myaesthenic syndrome</li><li>Anterior horn cell - spinal muscular atrophies if chronic, motor neuron disease if subacute and progressive}} | {{family tree | | D01 | | D02 | | | | D03 | | |D01=<ul><li>[[Myositis|Inflammatory myositis]]<ul><li>Polymyositis</li><li>dermatomyositis</li><li>immune mediated necrotising myopathy </li></ul></li><li>Endocrine - e.g cushings, dysthyroid</li>Drugs<li>Hyper/hypokalaemia</li></ul>|D02=<ul><li>Becker's or Duchenne's muscular dystrophy</li><li>Limb girdle muscle dystrophies</li><li>Congenital myopathies </li><li>Mitochondrial</li><li>Metabolic ([[Glycogen Storage Diseases|glycogen or lipid disorder]])</li><li>[[Pompe Disease|Acid maltase]]</li></ul>|D03=<ul><li>Peripheral neuropathies with proximal weakness - vasculitis or [[Chronic Inflammatory Demyelinating Polyneuropathy|CIDP]]</li><li>Plexopathies e.g. [[Diabetic Amyotrophy|diabetic amyotrophy]]</li><li>Infiltration nerve root - neoplastic meningitis</li><li>[[Cervical Myelopathy|Myelopathy]]</li><li>Neuromuscular junction - Lambert Eaton myaesthenic syndrome</li><li>Anterior horn cell - spinal muscular atrophies if chronic, motor neuron disease if subacute and progressive}} | ||
{{family tree/end}} | {{family tree/end}} | ||
[[Category:Presenting Complaints]] | [[Category:Presenting Complaints]] | ||
[[Category:Neurology]] | |||
[[Category:Neuromuscular Disorders]] | |||
Revision as of 05:51, 10 March 2023
This article is a stub.
Classification
| Proximal Weakness | |||||||||||||||||||||||||||||||||
| Myopathic | Non-Myopathic | ||||||||||||||||||||||||||||||||
| Acquired | Genetic | ||||||||||||||||||||||||||||||||
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