511 results
diagnosis management differential syndrome neurology algorithm endocrinology psychiatry disease msk comparison rheumatology treatment pediatrics clinical cardiology peds physicalexam table criteria
Iron Deficiency - Pathophysiology, Signs and Symptoms #Iron #Deficiency #Pathophysiology #diagnosis #Signs #Symptoms
Iron Deficiency ... - Pathophysiology ... , Signs and Symptoms ... #Pathophysiology ... #Symptoms
Gaucher Disease Pathophsiology • Lysosomal storage disorder • Deficiency of ß-glucocerebrosidase • Accumulation of glucosylceramide in macrophages Diagnosis
Gaucher Disease Pathophsiology ... storage disorder • Deficiency ... Disease #Diagnosis #Signs ... #Symptoms
Hypothyroid Myopathy Very common (up to 80% ) in patients with hypothyroidism Pathophysiology: • T4 deficiency leads to
hypothyroidism Pathophysiology ... : • T4 deficiency ... Hypothyroid #Myopathy #pathophysiology ... #signs #symptoms
Feedback Loop: Growth Hormone (GH) Growth Hormone: • Liver -> GHR activates JAK-STAT pathway -> Incr IGF1
activates lipolysis Signs ... /Symptoms: • GH ... deficiency: ... endocrinology #pathophysiology
Xeropthalmia: Pathogenesis and Ocular Manifestations Decr Visual pigment -> Keratinization, thickening & non-wetting of the conjunctiva
with vitamin A deficiency ... #Xeropthalmia #pathophysiology ... ophthalmology #diagnosis #signs ... #symptoms
Rickets and Osteomalacia: Pathogenesis and Clinical Findings • Calcification inhibitors (excess exposure to A1, Fluoride, etidronate)
D or Phosphate deficiency ... D Metabolism: Deficiency ... #Osteomalacia #pathophysiology ... #diagnosis #signs ... #symptoms
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-Hydroxylase Deficiency ... amount of enzyme deficiency ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology
IgA Vasculitis – Henoch Scholein Purpura: Pathogenesis and Clinical Findings - Infectious Agents - 50% have
Circulating galactose-deficient ... Deficiency in galactosylation ... HenochScholeinPurpura #Pathophysiology ... #Diagnosis #Signs ... #Symptoms
X-Linked Agammaglobulinemia: Pathogenesis and clinical findings The epidemiology of this disease is 1/340,000 births and roughly double
Signs of immunodeficiency ... antibodies) -> Complete deficiency ... humoral immunity Signs ... /Symptoms/Findings ... Agammaglobulinemia #XLinked #pathophysiology
Central Retinal Artery Occlusion: Pathogenesis and clinical findings • Inflammatory Disease: (i.e. GCA, SLE, GPA) ->
Protein C & S deficiency ... , ATIII deficiency ... Occlusion #CRAO #pathophysiology ... ophthalmology #diagnosis #signs ... #symptoms
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