Created at 3:29 p.m. Aug, 21, 2024
Author: mohannadkh10
Related Note: 1480549877323 1
Rationale for change

Make it up to the point, without a change in the meaning

Extra Extra
Text
Werdnig-Hoffmann syndrome (type 1 spinal muscular atrophy) is caused by a(n) {{c1::autosomal recessive}} inherited mutation in the SMN1 gene on chromosome {{c2::5q}}, which facilitates the assembly of {{c3::snRNPs}}
Lecture Notes
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Missed Questions
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Pathoma
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Boards and Beyond
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First Aid


Sketchy


Watch Spinal Muscular Atrophy, Amyotrophic Lateral Sclerosis (ALS) & Friedreich Ataxia
Sketchy 2
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Sketchy Extra
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Picmonic
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Pixorize
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Physeo
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Bootcamp
Watch associated Bootcamp video - Invasive Spinal Cord Disease: Werdnig-Hoffman Disease
OME

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#AK_Step2_v12::#AMBOSS::Q9auM5 #AK_Step2_v12::!Shelf::Neuro::no_dupes #AK_Step2_v12::#Resources_by_rotation::Neuro::step1_neuro::step_1_neuro_zanki #AK_Step1_v12::^Systems::Neuro::spinalcordlesions !AK_UpdateTags::Step1decks::Zanki-Step-Decks::Zanki-Neurology::Kaplan-Neuroscience #AK_Original_Decks::Step_1::Zanki_Step_Decks::Zanki_Neurology::Kaplan_Neuroscience #AK_Step1_v12::#Pathoma::17_Neuro::02_Spinal_Cord_Lesions #AK_Step1_v12::^Other::^EXPN::BGedit #AK_Step1_v12::^Other::^FA_Updates::FA2018 #AK_Step1_v12::#AMBOSS::mlaVxk #AK_Step1_v12::#OME::PreClinical::Neuroscience::Neuroscience_3::Motor_And_Sensory_Systems #AK_Step1_v12::^Systems::Neuro::neurology #AK_Step1_v12::#SketchyPath::13_Neuro::03_Spinal_Cord_&_Peripheral_Nerve::01_Spinal_Muscular_Atrophy,_Amyotrophic_Lateral_Sclerosis_(ALS)_&_Friedreich_Ataxia #AK_Step1_v12::#FirstAid::12_Neurology_and_Special_Senses::03_Pathology::30_Spinal_cord_lesions::02_Spinal_muscular_atrophy::*Werdnig-Hoffmann #AK_Step1_v12::#UWorld::Step::2036 #AK_Step1_v12::^Systems::Neuro::KaplanNeurology::04-Spinal_Cord_2 #AK_Step1_v12::#UWorld::COMLEX::25145 #AK_Step1_v12::^Other::^HighYield::5-LowYield #AK_Step2_v12::Original_decks::Zanki_Step_2::Neuro::Step_1_Neuro #AK_Step1_v12::#Bootcamp::Neurology::09_Invasive_Spinal_Cord_Disease::06_Werdnig_Hoffman_Disease