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diagnosis 21hydroxylasedeficiency 21ohd ceap classification cll disorders genetics hematology leukemia lymphocytic management oncology pediatrics peds sarcoidosis symptoms veins venous workup
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... cold & mottled skin ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
CEAP Classification of Chronic Venous Disorders Clinical: C0 - NO clinical signs C1 - Small
Classification of Chronic ... : C0 - NO clinical ... signs C1 - Small ... Perforating veins Pathophysiology ... Classification #Chronic
Chronic Lymphocytic Leukemia - Summary Cancer affecting lymphocytes/Mature B cell neoplasm • Lymphocytes accumulate in large numbers
Chronic Lymphocytic ... Orange or Hep C Clinical ... Physical Exam/Signs ... Hepatomegaly • Skin ... leukemia #CLL #Chronic
Sarcoidosis - Diagnosis and Management Summary Epidemiology 1) High incidence in Scandinavian countries (11-24 cases per 100,000 individuals
survival is 93-95% Pathophysiology ... renal failure Clinical ... Self-limiting, chronic ... nodes: 13-15%, skin ... Diagnosis #Management #Signs
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