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diagnosis management 21hydroxylasedeficiency amyotrophic barre cullen cullensign emergencymedicine endocrinology fm gbs genetics guillain icu image lateral pancreatitis pediatrics peds peritonitis
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 ... • This is also ... , vomiting • Late ... #pathophysiology
Cullen's sign. Lipase 1,781. Bruising in the skin around the umbilicus. This sign is named after
pancreatitis but can also ... Pathophysiology: ... pregnancy, or other causes ... #cullensign #em ... #peritonitis #IM
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
of the clinical ... lateral sclerosis Pathophysiology ... - Causes progressive ... features developing later ... Lateral #Sclerosis #neurology
Guillain-Barré Syndrome (GBS) Acute autoimmune demyelinating polyradiculoneuropathy that presents with rapidly progressive flaccid weakness Epidemiology: • Incidence: 1
Incidence: 1 to 2 cases ... transplantation CLINICAL ... the underlying pathophysiology ... Hospital of Baltimore IM ... diagnosis #management #neurology
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