23 results
diagnosis signs msk ophthalmology management cellulitis complications hypothyroid neurology physicalexam 21hydroxylasedeficiency 21ohd adhesivecapsulitis adrenal cah caudaequina causes centralretinalartery chagas clinical
Radiculopathy: Signs and Symptoms • Back/Neck Pain • Decr Range of motion • Abnormal posturing •
and Symptoms ... of motion • Abnormal ... proprioception and ... Radiculopathy #MSK ... #symptoms #pathophysiology
Stress Fracture: Pathogenesis and clinical findings Abnormal biomechanics, Repetitive impact activities => Repetitive subthreshold mechanical loading => Bone strain =>
: Pathogenesis and ... clinical findings Abnormal ... StressFractures #msk ... #orthopedics #pathophysiology ... #symptoms #signs
Congenital Adrenal Hyperplasia - 21-Hydroxylase Deficiency - Signs and Symptoms • Brain: Androgenization effects, Glucocorticoid effects,
Congenital Adrenal ... Hydroxylase Deficiency - Signs ... and Symptoms • ... Cardiovascular: Abnormal ... #endocrinology
Spondylolysis & Spondylolisthesis: Pathogenesis and Clinical Findings Pars interarticularis stress fracture (spondylolysis) - most frequently in the
: Pathogenesis and ... vertebrae • CT - collar ... Spondylolisthesis #MSK ... #diagnosis #pathophysiology ... #signs #symptoms
Systemic Lupus Erythematosus (SLE): Musculoskeletal Manifestations • Immune Complex Deposition - Arthralgia, Arthritis
Proximal Weakness, Normal ... demineralization, and ... Erythematosus #SLE #MSK ... Complications #pathophysiology ... #signs #symptoms
Hypothyroid Myopathy Very common (up to 80% ) in patients with hypothyroidism Pathophysiology: • T4 deficiency leads to
hypothyroidism Pathophysiology ... deficiency leads to abnormal ... glycolysis dependent) and ... #signs #symptoms ... #endocrinology
Cauda Equina Syndrome Causes: • Large lumbar degenerative disc herniation (central) • Severe lumbar spondylosis • Neoplasm
lumbar spine Signs ... Areflexia (loss of normal ... CaudaEquina #Syndrome #MSK ... #pathophysiology ... #signs
Seesaw nystagmus -> eye move in an opposed vertical fashion (one goes up while the other
a sequence of abnormal ... malformation, congenital ... Video by Kathleen ... ophthalmology #clinical #video ... #eye #ocular #PhysicalExam
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 21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
: Pathogenesis and ... also known as "congenital ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
Xeropthalmia: Pathogenesis and Ocular Manifestations Decr Visual pigment -> Keratinization, thickening & non-wetting of the conjunctiva
Ocular Manifestations ... Xerophthalmia - abnormal ... #Xeropthalmia #pathophysiology ... ophthalmology #diagnosis #signs ... #symptoms
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