21 results
differential management hematology pathophysiology treatment algorithm oncology signs symptoms syndrome syndromes anemia aplastic ascorbicacid b12 beriberi bleeding bruising capillary chronic
Causes of Neutropenia with Pancytopenia - Differential Diagnosis Algorithm Sequestration: • Splenomegaly Marrow Infiltration: • Hematologic and non-hematologic
Causes of Neutropenia ... - Differential Diagnosis ... Myelodysplasia Nutritional ... deficiency: • ... #Hematology
Refeeding Syndrome Overview What Is It? • Electrolyte/fluid shifts caused by initiation of nutrition in severely malnourished patient.
initiation of nutrition ... severe clinical ... Hypo-Mg2+ • Vitamin deficiency ... • Vitamin D deficiency ... #Differential #Diagnosis
Etiologies of Folate Deficiency • Decreased dietary intake - uncommon in this era • Increased requirements
Etiologies of Folate Deficiency ... folate that can cause ... develop folate deficiency ... #differential #diagnosis ... #hematology #nutrition
Cold Urticaria Prevalence - 0.05% in the population Disease onset - Mostly 2nd to 4th decades of life Causes
decades of life Causes ... and clinical associations ... Foods 6. ... , abdominal pain ... #rheumatology #
Causes of Petechial Rash - Differential Diagnosis Algorithm Pinpoint areas (less than 2 mm) of hemorrhage, which
Causes of Petechial ... - Differential Diagnosis ... Amyloidosis - Nutritional ... deficiency Work ... Skin biopsy • Abdominal
Bleeding and Bruising - Disorders of Hemostasis - Differential Diagnosis Framework == Quantitative or Qualitative defect in
- Differential Diagnosis ... discern these causes ... Ehlers Danlos Nutrition ... #Differential #Diagnosis ... #Hematology
Vitamin B12 (Cobalamin) Deficiency Etiology: • Vit B12 - aka cobalamin. Present in foods derived from animal
B12 (Cobalamin) Deficiency ... Present in foods ... • Common Causes ... intrinsic factor, IF) Clinical ... #nutrition
Thiamine Deficiency - Differential Diagnosis Framework and Clinical Manifestations Causes of Thiamine Deficiency: • Poor intake: - Diets
- Differential Diagnosis ... Framework and Clinical ... Manifestations Causes ... #Differential #Diagnosis ... syndromes #beriberi #nutrition
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
accumulation of clinical ... Assessment • Clinical ... Cellular immune deficiency ... Drugs, Unknown cause ... treatment #summary #rheumatology
IgA Vasculitis – Henoch Scholein Purpura: Pathogenesis and Clinical Findings - Infectious Agents - 50% have
Pathogenesis and Clinical ... Circulating galactose-deficient ... Deficiency in galactosylation ... 85%) - Colicky abdominal ... Pathophysiology #Diagnosis
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