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diagnosis causes infant 21hydroxylasedeficiency 21ohd acute adult cough cyanosis dehydration depressed distress endocrinology floppy genetics hypotonic lethargic management neonatal pathophysiology
Causes of Depressed / Lethargic Newborn - Differential Diagnosis Algorithm Maternal Related: • Drugs (Ex. SSRI) •
- Differential ... Diagnosis Algorithm ... • Anemia • Shock ... #Causes #Peds # ... Pediatrics
Practical Pediatric Viral Rash Algorithm Child presenting with rash and current/ recent symptoms of viral illness but
Practical Pediatric ... Viral Rash Algorithm ... five days and no signs ... / symptoms of sepsis ... #Pediatrics #Peds
Signs and Symptoms of Respiratory Distress Through the Years. #signs #symptoms #diagnosis #differential #neonatal #pediatrics #adult
Signs and Symptoms ... #signs #symptoms ... #diagnosis #differential ... #neonatal #pediatrics ... #adult #peds #pulmonary
Causes of Respiratory Distress in the Newborn - Differential Diagnosis Algorithm Premature Newborn - Normal CXR:
- Differential ... Diagnosis Algorithm ... #Differential # ... #Causes #Peds # ... Pediatrics
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features of shock ... #PhysicalExam #Signs ... #Symptoms #Shock ... #Dehydration #Peds ... #Pediatrics
Causes of Cyanosis in the Newborn - Differential Diagnosis Algorithm Peripheral Only: • Poor Perfusion • Acrocyanosis Hemoglobinopathy:
Cyanosis in the Newborn ... - Differential ... Diagnosis Algorithm ... #Causes #Peds # ... Pediatrics
Pediatric SVT - Management Algorithm Identify SVT: • HR not variable • Abrupt rate changes • Infants:
Pediatric SVT - ... Management Algorithm ... Signs of shock or ... tachycardia #Management #Algorithm ... #peds #Pediatric
Causes of Acute Pediatric Cough - Differential Diagnosis Algorithm No Fever, No Tachypnea - Normal Chest Auscultation
Causes of Acute Pediatric ... Cough - Differential ... Diagnosis Algorithm ... Bronchitis - No URTI Symptoms ... #Causes #Peds #
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... vomiting • Late (shock ... endocrinology #peds ... #pediatrics
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Infant (Floppy Newborn ... ) - Differential ... Diagnosis Algorithm ... #Causes #Peds # ... Pediatrics
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