5 results
diagnosis management 21hydroxylasedeficiency 21ohd als amyotrophic encephalopathy endocrinology gravis lateral myasthenia myelitis posterior pres reversible sclerosis syndrome transverse
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Myasthenia Gravis Overview Myasthenia Gravis is an autoimmune disorder of the postsynaptic neuromuscular junction. Ab to
life-threatening Differential ... test - Cogan sign ... - Peek sign ... immunosuppressants - Meds ... diagnosis #management #neurology
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
lateral sclerosis Pathophysiology ... - Causes progressive ... conditions listed in differential ... diagnosis column Treatment ... Lateral #Sclerosis #neurology
Posterior Reversible Encephalopathy Syndrome (PRES) Overview Clinico-Radiological Syndrome, characterized by: • Headache • Seizures • Altered mental
may precede the neurologic ... Etiology: • Pathophysiology ... Reversible course Differential ... the underlying cause ... • Treatment of
Transverse Myelitis Overview Focal inflammatory disorder of the spinal cord resulting in rapid onset of weakness, sensory
monophasic Pathophysiology ... • Bilateral signs ... • Infectious causes ... Transverse Myelitis Treatment ... #differential
No results found for "cerebellar causes pathophysiology differential pediatrics signs peds genetics treatment neurology"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #cerebellar #causes #pathophysiology #differential #pediatrics #signs #peds #genetics #treatment #neurology