16 results
The Febrile Child - some diagnostic clues to evaluating the febrile child.

#Febrile #Fever #Evaluation #Assessment #Signs
Evaluation #Assessment #Signs ... #Symptoms #PhysicalExam ... Diagnosis #Peds #Pediatrics
Tetralogy of Fallot 

1. Right ventricular outflow tract obstruction 

2. Right ventricular hypertrophy 

3. Ventricular septal
hypertrophy 3. ... #Fallot #Peds #Pediatrics ... #Cardiology #Signs ... #Symptoms #Diagnosis
Hypothyroidism – symptoms and signs.

Symptoms: 
Tiredness/malaise, 
Weight gain,
Anorexia,
Cold intolerance, 
Poor memory,
Change in appearance, 
Depression, 
Poor libido,
and signs. ... , Deafness Signs ... Hypothyroid #Features #Signs ... #PhysicalExam # ... Endocrinology
Trousseau's Sign in Hypocalcemia

Trousseau sign of latent tetany is a medical sign observed in patients with
Trousseau's Sign ... tetany is a medical sign ... To elicit the sign ... held in place for 3 ... #Trousseaus #Sign
Clinical features of shock from dehydration in an infant

Decreased level of consciousness 
Sunken fontanelle 
Dry mucous
Extremities #PhysicalExam ... #Signs #Symptoms ... Dehydration #Peds #Pediatrics
Lancisi's sign in Severe Tricuspid Regurgitation - Physical Exam
Note the large systolic jugular venous wave caused
Lancisi's sign in ... IJ vein seen on POCUS ... rhythm (initial 3 ... #Lancisis #sign ... Regurgitation #PhysicalExam
Primary Adrenal Insufficiency
Addison's Disease - Damage of the adrenal glands with lack of cortisol, androgens and
vomiting • Fatigue Signs ... Cortisol Deficiency: Signs ... Reduced libido • Signs ... Serum cortisol < 3 ... #diagnosis #signs
Hypothyroidism and Hyperthyroidism - Symptoms and Signs
Hypothyroidism:
 - General - From asymptomatic to myxedema coma, “Like
Hyperthyroidism - Symptoms ... and Signs Hypothyroidism ... Thinning of lateral 1/3 ... #Signs #Diagnosis ... #endocrinology
Classic Findings During Hallpike Test in Posterior Canal Benign Paroxysmal Positional Vertigo (BPPV)
 • Latency (delay
approximately 3 ... Reproduction of vertigo symptoms ... #dixhallpike #physicalexam ... testing #findings #signs
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... pathophysiology #genetics #endocrinology ... #peds #pediatrics