19 results
diagnosis peds differential causes management signs treatment iem inbornerrors metabolism neonatology nicu syndrome table 21hydroxylasedeficiency 21ohd acromegaly acute adrenal anorexianervosa
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
schema of the pathophysiology ... , UpToDate #Pediatrics ... MetabolicEmergency #Genetics ... #Pathophysiology ... #Diagnosis #Algorithm
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... #causes #pediatrics ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
Lab patterns seen in Inborn Errors of Metabolism A table of lab values compiled from UpToDate and
from UpToDate and Pediatrics ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... Neonatology #Peds #Pediatrics ... #Table #NICU #Genetics
Causes of Acute Pediatric Cough - Differential Diagnosis Algorithm No Fever, No Tachypnea - Normal Chest Auscultation
Causes of Acute Pediatric ... Differential Diagnosis Algorithm ... Tachypnea - Normal ... Bronchitis - No URTI Symptoms ... Tachypnea - Normal
Functional Dyspepsia - Pathophysiology, Diagnosis and Management Risk factors: Non-steroidal anti-inflammatory drugs, Psychological comorbidity, Helicobacter pylori infection,
Functional Dyspepsia - Pathophysiology ... sex, Smoking Symptoms ... : Bothersome symptoms ... a structurally normal ... Diagnosis #Management #algorithm
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Syndrome Signs/Symptoms ... PraderWilli #Syndrome #genetics ... #pathophysiology ... #peds #pediatrics
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Differential Diagnosis Algorithm ... Normal Variant ... Differential #Diagnosis #Algorithm ... #endocrinology ... #causes #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Causes of Growth Restriction - Small for Gestational Age - Differential Diagnosis Algorithm Maternal • Chronic Maternal
Differential Diagnosis Algorithm ... Chromosomal Anomaly • Genetic ... Placenta Previa • Abnormal ... Differential #Diagnosis #Algorithm ... Causes #Obstetrics #Pediatrics
Hypocalcemia - Differential Diagnosis Algorithm - Low and High PTH LOW PTH - Hypoparathyroid - Congenital (Pediatric)
Differential Diagnosis Algorithm ... - Congenital (Pediatric ... rhabdomyolysis, oral ... Differential #Diagnosis #Algorithm ... #PTH #endocrinology
No results found for "Normal pathophysiology symptoms algorithm pediatrics endocrinology genetics"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #Normal #pathophysiology #symptoms #algorithm #pediatrics #endocrinology #genetics