45 results
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
algorithm #causes #pediatrics ... comparison #treatment #Peds ... #Endocrinology ... #Adrenal #pathophysiology
Bronchiolitis - Pathophysiology and Clinical Features

#Pediatrics #Peds #Pathophysiology #Bronchiolitis
Bronchiolitis - Pathophysiology ... and Clinical Features ... #Pediatrics # ... Peds #Pathophysiology
Pediatric Discitis - Inflammation of intervertebral disc 
Etiology 
 • Bacterial or viral 
Clinical 
 •
Pediatric Discitis ... Bacterial or viral Clinical ... • Radicular symptoms ... intervertebral #Pediatrics ... #Peds #Diagnosis
Brudzinski's Sign on Physical Exam - Meningitis

#Brudzinskis #Sign #PhysicalExam #clinical #video #neurology #peds #pediatrics #meningitis
#PhysicalExam #clinical ... #video #neurology ... #peds #pediatrics
Pediatric Parasomnias and Nightmares: Pathogenesis and clinical findings

Parasomnias - Micro-arousal episodes during SWS ->
Intense activation of
Pediatric Parasomnias ... Pathogenesis and clinical ... Parasomnias #Nightmares #Pediatrics ... #Peds #pathophysiology ... #symptoms #pharmacology
Aortic Stenosis & Bicuspid Aortic Valve (AS)
 • Introduction & Pathophysiology
 • Classifications
 • Epidemiology
 •
Introduction & Pathophysiology ... Epidemiology • Clinical ... AorticValve #cardiology #peds ... #pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... • Deletion of critical ... Syndrome Signs/Symptoms ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Scarlet Fever - Other symptoms include: white coating on the tongue which then peels and leave
Fever - Other symptoms ... lymphadenopathy #Clinical ... #Dermatology #Peds ... #Pediatrics #SkinRash
Nuchal Rigidity in Infantile Bacterial Meningitis

Flexion of the neck revealed nuchal rigidity. The patient was unable
From - Journal of Pediatrics ... #PhysicalExam #Clinical ... #Video #Peds #Pediatrics ... #neurology
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 ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics