8 results
diagnosis differential pediatrics constipation 21hydroxylasedeficiency 21ohd acth adrenal amenorrhea asthma floppy genetics hypotonic infant insufficiency neurology neuromuscular newborn pathophysiology pediatric
Pulmonary Function Testing (PFT) Interpretation Algorithm Restrictive Lung Disease: • Chest wall or neuromuscular disorders • Interstitial
Pulmonary Function ... Testing (PFT) Interpretation ... Algorithm Restrictive ... #Testing #PFT # ... PFTs #Interpretation
Causes of Pediatric Constipation - Differential Diagnosis Algorithm Dietary / Functional: • Insufficient Volume / Bulk Neurologic: •
Causes of Pediatric ... Differential Diagnosis Algorithm ... Dietary / Functional ... Disease • Spinal Cord ... #Causes #Peds #
Pediatric Constipation - Differential Diagnosis Algorithm Dietary/Functional • lnsufficient Volume / Bulk Neurologic • Hirschsprung's Disease • Imperforate
Differential Diagnosis Algorithm ... Dietary/Functional ... Atresia Dietary/Functional ... Disease • Spinal Cord ... #Causes #Peds
Amenorrhea - Differential Diagnosis Algorithm Elevated FSH • Premature Ovarian Failure • Menopa use • Spontaneous Bleed With
Differential Diagnosis Algorithm ... Challenge • Functional ... • Weight Loss, Eating ... #endocrinology ... #causes
Causes of Neuromuscular Weakness • Spinal Cord: Demyelinating Disease (MS), Epidural abscess, Infarction, Syringomyelia, Tetanus, Transverse
Causes of Neuromuscular ... Weakness • Spinal Cord ... Neuromuscular junction ... poisoning, Scorpion sting ... Shellfish poisoning, Meds
Adrenal Insufficiency Diagnosis Algorithm - Evaluation of HPA Axis Response to ACTH Early am cortisol < 3
Insufficiency Diagnosis Algorithm ... unclear (often the case ... then go to stim testing ... normal adrenal function ... Stimulation #Test #Endocrinology
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic ... Differential Diagnosis Algorithm ... Syndromes - Spinal Cord ... Neuromuscular Junction ... #Causes #Peds #
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... glands • Salt wasting ... Late (shock): cold ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
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