14 results
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... findings • Maternal ... Prader-Willi Syndrome Signs ... pathophysiology #peds ... #pediatrics
Combination of Skin Findings and Arthritis in Pediatrics Patient - Differential Diagnosis
Malar rash: 
 • A
Combination of Skin Findings ... Pediatrics Patient ... not be seen try focus ... migrans: • Target sign ... #peds #pediatrics
Bilateral B-Lines in case of Pneumonia on Lung POCUS

Young healthy pt with fever/dyspnea. POCUS lung exam
POCUS lung exam ... Lung POCUS shows ... partially seen shred sign ... NOT definitively diagnose ... #POCUS #clinical
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Findings Autosomal ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
Clinical features of Liver Disease in Children

#Cirrhosis #LiverFailure #Signs #Symptoms #PhysicalExam #Findings #Diagnosis #Peds #Pediatrics #Hepatology

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Clinical features ... #LiverFailure #Signs ... #Symptoms #PhysicalExam ... #Findings #Diagnosis ... #Peds #Pediatrics
Clinical Manifestations and Diagnosis of Lyme Disease - Borreliosis
Erythema migrans
 - 3-32 days (median: 7-10 days)
Clinical Manifestations ... and Diagnosis of ... specific laboratory findings ... #Borreliosis #Diagnosis ... #Signs #Symptoms
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children)
Upper Respiratory Tract Infection: 
 - Bacterial: Streptococcus
Pathogenesis and Clinical ... Findings (in Children ... pathophysiology #diagnosis ... #symptoms #signs ... #peds #pediatrics
Joint Approach to Juvenile Idiopathic Arthritis (JIA)
JIA is a clinical diagnosis - Diagnostic criteria:
 • One
(JIA) JIA is a clinical ... diagnosis - Diagnostic ... symmetry • Look for signs ... #JIA #pediatrics ... #peds #diagnosis
Myasthenia Gravis Overview

Myasthenia Gravis is an autoimmune disorder of the postsynaptic neuromuscular junction.  Ab to
syndrome, rheumatoid arthritis ... myasthenia Diagnosis ... and EMG Findings ... test - Cogan sign ... - Peek sign
Evaluation of suspected incomplete Kawasaki Disease

1. AHA consensus recommendations
2. Infants ≤6 months old on day ≥7
if they have no clinical ... Check for classic findings ... and lab signs ( ... #Diagnosis #Peds ... #Pediatrics #Kawasaki