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diagnosis differential peds adrenal constipation guillain management neurology pathophysiology syndrome treatment 21hydroxylasedeficiency 21ohd acth cah comparison congenitaladrenalhyperplasia gbs genetics guillainbarre
Causes of Pediatric Constipation - Differential Diagnosis Algorithm Dietary / Functional: • Insufficient Volume / Bulk Neurologic: •
Causes of Pediatric ... Differential Diagnosis Algorithm ... Congenita • Guillain-Barré ... #Causes #Peds # ... Pediatrics
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... #causes #pediatrics ... treatment #Peds #Endocrinology
Guillain-Barre Syndrome - Summary Acute AIDP that presents with rapidly progressive flaccid weakness Epidemiology: • 1-2 cases/100,000 per
Guillain-Barre Syndrome ... Epidemiology: • 1-2 cases ... females Guillain-Barre ... with walking to nearly ... Albuminocytologic dissociation
Tall Stature - Differential Diagnosis Algorithm Normal Growth (BA=CA) • Familial Tall Stature • XYY Syndrome Obese BMI
Differential Diagnosis Algorithm ... Tall Stature (Early ... Differential #Diagnosis #Algorithm ... #endocrinology ... #causes
Adrenal Insufficiency Diagnosis Algorithm - Evaluation of HPA Axis Response to ACTH Early am cortisol < 3
Insufficiency Diagnosis Algorithm ... Response to ACTH Early ... unclear (often the case ... Insufficiency #Diagnosis #Algorithm ... Stimulation #Test #Endocrinology
Guillain-Barré Syndrome (GBS) Acute autoimmune demyelinating polyradiculoneuropathy that presents with rapidly progressive flaccid weakness Epidemiology: • Incidence: 1
Guillain-Barré Syndrome ... Incidence: 1 to 2 cases ... with walking to nearly ... albuminocytologic dissociation ... GBS #Guillain #Barre
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
Differential Diagnosis Algorithm ... 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
enzyme 21-OHase causes ... Hypoglycemia • Early ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Pediatric Constipation - Differential Diagnosis Algorithm Dietary/Functional • lnsufficient Volume / Bulk Neurologic • Hirschsprung's Disease • Imperforate
Pediatric Constipation ... Differential Diagnosis Algorithm ... Congenita • Guillan-Barré ... #Constipation #Pediatric ... #Causes #Peds
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