What Genetic Expansion Causes Myotonic Dystrophy (DM1 & DM2)? - Muscular Dystrophy Support Network
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What Genetic Expansion Causes Myotonic Dystrophy (DM1 & DM2)…
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YouTubeMuscular Dystrophy Support Network
Neurology physical examination on Instagram: "Myotonic Dystrophy (DM) – Detailed Explanation Myotonic dystrophy is a genetic, multisystem, progressive neuromuscular disorder characterized by: 1. Myotonia – delayed relaxation of muscles after contraction 2. Muscle weakness and wasting 3. Systemic involvement – eyes, heart, endocrine system, GI tract, CNS, etc. It is the most common adult-onset muscular dystrophy. --- TYPES 1. Myotonic Dystrophy Type 1 (DM1 / Steinert Disease) Caused by CTG trinuc
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Neurology physical examination on Instagram: "Myotonic Dystrophy (…
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Instagramdr._neuro.2025
✅🧑‍⚕️👩🏻‍⚕️Let’s review the Pathophysiology & clinical manifestations of DKA! Full DKA breakdown in my study guide. ⬆️ . ➡️Follow for part 2! . 🤢😷DKA occurs in type 1 diabetics, usually following an illness. The body is stressed & blood glucose rises. . 🍩🍪🍰Since type 1 diabetics do not produce insulin, this causes their bodies to switch to using fat for energy. This is called lipolysis. Lipolysis leads to increased circulating ketones & metabolic acidosis. . 😮‍💨DKA patients will hyperve
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✅🧑‍⚕️👩🏻‍⚕️Let’s review the Pathophysiology & clinical manife…
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TikToknursingschool911
Neurology physical examination on Instagram: "Myotonic Dystrophy (DM) – Detailed Explanation Myotonic dystrophy is a genetic, multisystem, progressive neuromuscular disorder characterized by: Myotonia – delayed relaxation of muscles after contraction Muscle weakness and wasting Systemic involvement – eyes, heart, endocrine system, GI tract, CNS, etc. It is the most common adult-onset muscular dystrophy. TYPES 1. Myotonic Dystrophy Type 1 (DM1 / Steinert Disease) Caused by CTG trinucleotide repea
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Neurology physical examination on Instagram: "Myotonic Dystrophy (…
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Instagramdr._neuro.2025
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