12 results
diagnosis pediatrics differential management symptoms genetics neurology treatment 21hydroxylasedeficiency 21ohd adrenal cah cardiology chf clinical comparison congenitaladrenalhyperplasia criticalcare embolism encephalopathy
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
Causes of Pediatric Wheezing - Differential Diagnosis Algorithm CXR Abnormal: • Pulmonary Sequestration • Congenital Adenoid Cystic
Causes of Pediatric ... Differential Diagnosis Algorithm ... Abnormal: • Pulmonary ... Vascular Compression Syndrome ... #Causes #Peds #
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... Signs/Symptoms ... sleep apnea, cor pulmonale ... #genetics #pathophysiology ... #peds #pediatrics
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm Congenital Anomaly / Disorder: •
Causes of Sudden ... Differential Diagnosis Algorithm ... Neurologic Anomaly • Pulmonary ... Sudden Infant Death Syndrome ... #Causes #Peds #
Fat Embolism Syndrome Trauma to the long bone or pelvis accounts for —9096 of cases. The diagnosis
Fat Embolism Syndrome ... accounts for —9096 of cases ... Pathophysiology ... onset widespread pulmonary ... #Diagnosis #Signs
Hyponatremia - Differential Diagnosis Algorithm Hypovolemic - Give volume Hypervolemic (Edematous) - Look for and treat underlying cause
Differential Diagnosis Algorithm ... treat underlying cause ... cirrhosis, nephrotic syndrome ... Pulmonary Diseases ... , CNS Disease, Meds
Growth Hormone Excess - Pathogenesis and clinical findings • Acromegaly and gigantism share the same pathophysiology
• Other rare causes ... Carpal Tunnel Syndrome ... Overproduction #diagnosis #signs ... #symptoms #endocrinology ... #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 ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Sarcoidosis - Diagnosis and Management Summary Epidemiology 1) High incidence in Scandinavian countries (11-24 cases per 100,000 individuals
survival is 93-95% Pathophysiology ... Pulmonary: dyspnea ... acute sarcoidosis Pulmonary ... • Heerfordt syndrome ... Diagnosis #Management #Signs
Myasthenia Gravis Overview Myasthenia Gravis is an autoimmune disorder of the postsynaptic neuromuscular junction. Ab to
Myasthenia Gravis Overview ... test - Cogan sign ... - Peek sign ... Myasthenia Crises ... immunosuppressants - Meds
No results found for "Overview pathophysiology signs syndrome causes algorithm pulmonary peds endocrinology"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #Overview #pathophysiology #signs #syndrome #causes #algorithm #pulmonary #peds #endocrinology