10 results
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm
Congenital Anomaly / Disorder:
 •
Unexpected Death in Infancy ... - Differential Diagnosis ... Algorithm Congenital ... #Diagnosis #Algorithm ... #Causes #Peds #Pediatrics
Causes of Pediatric Seizures - Differential Diagnosis Algorithm
Infantile:
 • Benign Focal Epilepsy of Infancy
 • West
Causes of Pediatric ... - Differential Diagnosis ... • Tumours • Congenital ... #Differential #Diagnosis ... #Causes #Peds #Pediatrics
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
various types of congenital ... algorithm #causes #pediatrics ... CongenitalAdrenalHyperplasia #diagnosis ... treatment #Peds #Endocrinology
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm
Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic Infant ... - Differential Diagnosis ... #Hypotonic #Infant ... #Differential #Diagnosis ... #Causes #Peds #Pediatrics
Benign Adrenal Mass - Differential Diagnosis Algorithm
Hyperplasia - Often Bilateral
 • Congenital Adrenal Hyperplasia
 • ACTH
- Differential Diagnosis ... Bilateral • Congenital ... • Other #AdrenalMass ... #Differential #Diagnosis ... #Algorithm #Endocrinology
Malignant Adrenal Mass - Differential Diagnosis Algorithm
Suggestive of Malignancy: Inhomogenous Density, Delay in CT Contrast Washout
- Differential Diagnosis ... Ovarian Syndrome, Congenital ... Carcinoma #AdrenalMass ... #Differential #Diagnosis ... #Algorithm #Endocrinology
Hypocalcemia - Differential Diagnosis Algorithm - Low and High PTH
LOW PTH - Hypoparathyroid
 - Congenital (Pediatric)
- Differential Diagnosis ... Hypoparathyroid - Congenital ... (Pediatric) ... #Differential #Diagnosis ... Algorithm #PTH #endocrinology
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm
Cardiac:
 • Congenital Heart Disease
 •
- Differential Diagnosis ... Cardiac: • Congenital ... Breathing • Apnea of Infancy ... #Differential #Diagnosis ... #Causes #Peds #Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
also known as "congenital ... deficiencies present in infants ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Short Stature - Differential Diagnosis Algorithm
Normal Variant, Normal Puberty Onset (BA = CA)
 • Familial Short
- Differential Diagnosis ... Hypothyroidism • Congenital ... #Differential #Diagnosis ... #Algorithm #endocrinology ... #causes #pediatrics