22 results
Signs and Symptoms of Respiratory Distress Through the Years. 

#signs #symptoms #diagnosis #differential #neonatal #pediatrics #adult
Signs and Symptoms ... #signs #symptoms ... differential #neonatal #pediatrics ... #adult #peds #pulmonary ... respiratory #distress #causes
Paradoxical Breathing on Physical Exam

Paradoxical breathing is often a sign of breathing problems. It causes the
breathing is often a sign ... It causes the chest ... respiratory #clinical #video ... #pulmonary #peds ... #pediatrics
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Epiglottitis - Swollen inflamed epiglottis 
Clinical (Rapid onset) 
 • Fever 
 • Sore throat
#Epiglottitis #Signs ... #Causes #Diagnosis ... #Differential #Peds ... #Pediatrics
The Febrile Child - some diagnostic clues to evaluating the febrile child.

#Febrile #Fever #Evaluation #Assessment #Signs
some diagnostic clues ... Evaluation #Assessment #Signs ... PhysicalExam #Diagnosis #Peds ... #Pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski)

Brudzinski's sign is characterized
Passive neck flexion causes ... Video by Dr. ... Meningitis #Clinical #Video ... #PhysicalExam #Pediatrics ... #Peds
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Assessment of the Child with Chronic Asthma
Are there other allergic disorders?
 - Allergic rhinitis
 - Eczema,
Other causes should ... Assessment #diagnosis #peds ... #pediatrics #primarycare
THE LIMPING OR NON-WEIGHT BEARING CHILD PATHWAY

RED FLAGS - In all cases there are specific
markers which
FLAGS - In all cases ... disease and these should ... Pathway #Child #Peds ... #Pediatrics #Diagnosis
Gowers' Sign on Physical Exam

Caused by proximal muscle weakness typically seen in muscular dystrophy

#Gowers #Sign #PhysicalExam
Gowers' Sign on ... Physical Exam Caused ... dystrophy #Gowers #Sign ... neurology #clinical #video ... #pediatrics #muscular
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DKA DIAGNOSTIC CRITERIA:
1. Serum glucose >250 mg/dL
2. Arterial pH <7.3
3. Serum bicarbonate <18 mEq/L
4. At least
Arterial pH <7.3 ... to 30% of DKA cases ... infection, antibiotics should ... Common, early signs ... resuscitation should
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics