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diagnosis differential pediatrics adrenal management 21hydroxylasedeficiency 21ohd ai anosmia cah comparison congenitaladrenalhyperplasia encephalopathy erectile genetics glftap insufficiency loss macroadenoma male
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
#CAH #algorithm ... #causes #pediatrics ... comparison #treatment #Peds ... #Endocrinology ... #Adrenal #pathophysiology
Anosmia / Smell Dysfunction - Differential Diagnosis Algorithm Nasal Obstruction/ URTI: • Septal Deviation • Allergic Rhinitis
Anosmia / Smell Dysfunction ... Differential Diagnosis Algorithm ... • Adrenal Hyperfunction ... Anosmia #Smelling #Dysfunction ... #Causes
Causes of Pediatric Stridor - Differential Diagnosis Algorithm Present Since Infancy with No Respiratory Distress: • Laryngomalacia Present
Causes of Pediatric ... Differential Diagnosis Algorithm ... • Vocal Cord Dysfunction ... • Vocal Cord Dysfunction ... #Causes #Peds #
Causes of Adrenal Insufficiency - Differential Diagnosis Algorithm ACTH-Dependent (Secondary): • Pituitary Dysfunction • Hypothalamic Dysfunction ACTH-Independent (Primary):
Causes of Adrenal ... Differential Diagnosis Algorithm ... : • Pituitary Dysfunction ... • Hypothalamic Dysfunction ... #Causes #endocrinology
Male Sexual and Erectile Dysfunction - Differential Diagnosis Algorithm Erectile Dysfunction - Psychological •
Differential Diagnosis Algorithm ... Erectile Dysfunction ... Differential #Diagnosis #Algorithm ... #endocrinology ... #causes
SEPSIS AND SEPTIC SHOCK DEFINITION AND PATHOPHYSIOLOGY • Sepsis: Life-threatening organ dysfunction due to a dysregulated host
DEFINITION AND PATHOPHYSIOLOGY ... • Pathophysiology ... • 49 million cases ... /hypofunction. ... COMMON CAUSES +
Pituitary Mass Effects - Pathogenesis and Clinical Findings • Pituitary turnors are almost always a benign
For pituitary masses ... Headaches • Nausea ... • Hypothalamic dysfunction ... #SideEffects #endocrinology ... mnemonic #GLFTAP #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Posterior Reversible Encephalopathy Syndrome (PRES) Overview Clinico-Radiological Syndrome, characterized by: • Headache • Seizures • Altered mental
Etiology: • Pathophysiology ... unclear, endothelial dysfunction ... the underlying cause ... Seizures: Treat with AEDs ... until cause identified
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