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pathophysiology 21hydroxylasedeficiency buckethandle differential endocrinology gait genetics gravis knee management medial meniscus mri myasthenia neuromuscular symptoms tear trendelenburg weakness
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Causes of Neuromuscular Weakness • Spinal Cord: Demyelinating Disease (MS), Epidural abscess, Infarction, Syringomyelia, Tetanus, Transverse
Causes of Neuromuscular ... Demyelinating Disease (MS ... Mitochondrial myopathy, Muscular ... #differential #diagnosis ... #neurology
Trendelenburg Gait: Pathogenesis and clinical findings Skeletal Pathology of the Hip • Arthritis • Congenital hip dysplasia
Pathogenesis and clinical ... Chondrodysplasia Neurologic ... • Compensatory muscular ... #symptoms #signs ... #diagnosis #msk
Medial Meniscus Bucket Handle Tear - MSK Radiology Imaging Findings: • Truncation of the medial meniscus on
Handle Tear - MSK ... The "double PCL sign ... Case description ... Tear #knee #mri #clinical ... #Radiology #diagnosis
Myasthenia Gravis Overview Myasthenia Gravis is an autoimmune disorder of the postsynaptic neuromuscular junction. Ab to
myasthenia Diagnosis ... test - Cogan sign ... - Peek sign ... Myasthenia #Gravis #diagnosis ... #management #neurology
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