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diagnosis algorithm 21hydroxylasedeficiency 21ohd cah comparison congenitaladrenalhyperplasia differential encephalopathy examination genetics infant management neurology newborn physicalexam posterior pres reversible shortstature
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
CAH #algorithm #causes ... #pediatrics #CongenitalAdrenalHyperplasia ... diagnosis #comparison #treatment ... #Peds #Endocrinology ... #Adrenal #pathophysiology
Short Stature - Differential Diagnosis Algorithm Normal Variant, Normal Puberty Onset (BA = CA) • Familial Short
• Congenital Adrenal ... Panhypopituitarism Treatment ... Celiac, IBD) • Renal ... 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 ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Posterior Reversible Encephalopathy Syndrome (PRES) Overview Clinico-Radiological Syndrome, characterized by: • Headache • Seizures • Altered mental
Etiology: • Pathophysiology ... epilepticus Treatment ... the underlying cause ... • Treatment of ... until cause identified
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
is also a late sign ... are observed for signs ... intra-abdominal masses ... #Examination #Peds ... #Pediatrics #Diagnosis
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