21 results
signs pathophysiology peds rheumatology disease differential management treatment vasculitis 21hydroxylasedeficiency 21ohd addisons adverse aion algorithm anteriorischemicopticneuropathy cah cardiology cellulitis centralretinalartery
Tetralogy of Fallot 1. Right ventricular outflow tract obstruction 2. Right ventricular hypertrophy 3. Ventricular septal
Ventricular septal defect ... #Fallot #Peds #Pediatrics ... #Cardiology #Signs ... #Symptoms #Diagnosis
Congenital Adrenal Hyperplasia - 21-Hydroxylase Deficiency - Signs and Symptoms • Brain: Androgenization effects, Glucocorticoid effects,
Hydroxylase Deficiency - Signs ... and Symptoms • ... Hydroxylase #Deficiency #Signs ... #Symptoms #diagnosis ... #endocrinology
Cirrhosis - Illustrated signs and symptoms: Integumentary, neurologic, gastrointestinal, portal hypertension effects, hematologic, renal, metabolic, cardiovascular, reproductive #Diagnosis
- Illustrated signs ... and symptoms: ... portal hypertension effects ... , hematologic, renal ... #Cirrhosis #Signs
Exogenous Testosterone Side Effects • Mood disorder, Depression, Aggression • ↑ Erythropoiesis • Hypogonadism +/-BPH, prostate
Testosterone Side Effects ... SideEffects #adverse #diagnosis ... #signs #symptoms ... #steroids #endocrinology
Primary Adrenal Insufficiency Addison's Disease - Damage of the adrenal glands with lack of cortisol, androgens and
vomiting • Fatigue Signs ... Reduced libido • Signs ... Serum DHEAS Diagnosis ... addisons #disease #endocrinology ... #diagnosis #signs
Clinical Effects of Large and Small Pituitary Tumours Local complications - Headache, Visual field defect, Disconnection hyperprolactinaemia,
Clinical Effects ... , Visual field defect ... Pituitary #Tumors #Signs ... #Symptoms #Diagnosis ... #Endocrinology
Kawasaki Disease (Mucocutaneous Lymph Node Syndrome) An rare systemic acute febrile vasculitic syndrome. Aetiology unknown. Affects
Affects children ... Early diagnosis ... Disease #Features #Signs ... #Symptoms #Diagnosis ... #Peds #Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-OHD in the adrenal ... as "congenital adrenal ... Signs/Symptoms/Complications ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Anterior ischemic optic neuropathy (AION) - Recognition of giant cell arteritis (GCA) 1) Is visual loss caused
field: altitudinal defect ... • Cephalic symptoms ... Doppler US : halo sign ... #Rheumatology #Ophthalmology ... #Diagnosis #Algorithm
Clinical Features of Systemic Lupus (SLE) General: Fever (50%), Depression, Fatigue (75%), Weight loss (50%) Eye: Sjögrens (15%) Skin
Restrictive lung defect ... Abdominal pain (20%) Renal ... erythematosus #signs ... #symptoms #diagnosis
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