36 results
neurology disease febrile fever hematology infant pathophysiology syndrome antibiotics arthritis cardiology differential genetics hemophagocytic hlh lp lymphohistiocytosis pneumonia pulmonary rheumatology
Practical Pediatric Viral Rash Algorithm Child presenting with rash and current/ recent symptoms of viral illness but
Practical Pediatric ... Viral Rash Algorithm ... five days and no signs ... #Pediatrics #Peds ... #Diagnosis
Pediatric SVT - Management Algorithm Identify SVT: • HR not variable • Abrupt rate changes • Infants:
Pediatric SVT - ... Management Algorithm ... Signs of shock or ... #Algorithm #peds ... #Pediatric #treatment
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Prader-Willi Syndrome Signs ... /Symptoms/Complications ... pathophysiology #peds ... #pediatrics
Cor triatriatum • Epidemiology • Etiology • Associated Lesions • Differentials Diagnosis • Anatomy - Sinister,
Physiology • Clinical ... • Treatment ... Post-Operative Management ... #summary #peds ... #pediatrics
Clinical Features and Complications of Measles Rash: Spreads downwards, from behind the ears to the whole Of the
Clinical Features ... #Measles #Diagnosis ... Kopliks KoplikSpots #Peds ... #Pediatrics #Timeline ... #Signs #Symptoms
Clinical Algorithm for Emergency Department Evaluation and Management of UTI in Febrile Infants and Young Children Urinary
Clinical Algorithm ... Evaluation and Management ... do not replace clinical ... #Diagnosis #Management ... Febrile #Infant #Peds
Bronchiolitis Bronchiolitis is a viral inflamation of the bronchioles and the commonest LRTI in under 1s'. It's
Diagnosis - Coryzal ... symptoms for 1 ... Bronchiolitis #pediatrics ... #diagnosis #management ... #peds #treatment
Polycythemia Vera (PV) - Diagnosis and Management Summary Diagnostic Criteria: • Elevated hemoglobin and/or hematocrit AND •
and Management ... Summary Diagnostic ... , signs, and complications ... • Treatment algorithms ... #Management #Summary
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 ... Hirsutism & acne • Infertility ... endocrinology #peds ... #pediatrics
“Step by Step” – the new kid on the block – aims to risk stratify this
investigations and treatments ... components of the algorithm ... CRP < 20 mg/L #Diagnosis ... #Management #Pediatrics ... #Peds #Febrile
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