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diagnosis algorithm peds infancy 21hydroxylasedeficiency 21ohd alte brue comparison epilepsy event floppy genetics hypocalcemia hypokalemia hypotonic lifethreatening lowcalcium newborn pathophysiology
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm Congenital Anomaly / Disorder: •
Causes of Sudden ... (SUDI) - Differential ... Diagnosis Algorithm Congenital ... #Infant #Differential ... #Peds #Pediatrics
Causes of Pediatric Seizures - Differential Diagnosis Algorithm Infantile: • Benign Focal Epilepsy of Infancy • West
Causes of Pediatric ... Seizures - Differential ... • Tumours • Congenital ... Diagnosis #Algorithm #Causes ... #Peds #Pediatrics
Comparison of Causes of Salt-Wasting in Infancy - PHA 1 - PHA 3 - 21-OH CAH
Comparison of Causes ... Salt-Wasting in Infancy ... #differential # ... diagnosis #pediatrics ... #nephrology
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Differential Diagnosis ... Hypothyroidism • Congenital ... #ShortStature #Differential ... Diagnosis #Algorithm #endocrinology ... #causes #pediatrics
Hypocalcemia - Differential Diagnosis Algorithm - Low and High PTH LOW PTH - Hypoparathyroid - Congenital (Pediatric)
Hypocalcemia - Differential ... Hypoparathyroid - Congenital ... (Pediatric) ... Malabsorption • Short ... Algorithm #PTH #endocrinology
Causes of Hypokalemia - Differential Diagnosis Algorithm Defining the cause of hypokalemia starts by measuring urinary K
- Differential ... of hypokalemia starts ... Liddle's syndrome, Congenital ... #hypokalemia #differential ... #nephrology #potassium
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm Cardiac: • Congenital Heart Disease •
Causes of Apparent ... Event (ALTE) - Differential ... Cardiac: • Congenital ... Breathing • Apnea of Infancy ... #Peds #Pediatrics
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic ... Infant (Floppy ... Newborn) - Differential ... #Hypotonic #Infant ... #Peds #Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... also known as "congenital ... deficiencies present in infants ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
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