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diagnosis causes differential infant genetics pathophysiology physicalexam 21hydroxylasedeficiency 21ohd dehydration depressed disease endocrinology examination features floppy hypotonic inflammatory kawasaki lethargic
Causes of Depressed / Lethargic Newborn - Differential Diagnosis Algorithm Maternal Related: • Drugs (Ex. SSRI) •
Depressed / Lethargic Newborn ... Respiratory Distress Syndrome ... • Anemia • Shock ... #Causes #Peds # ... Pediatrics
Causes of Respiratory Distress in the Newborn - Differential Diagnosis Algorithm Premature Newborn - Normal CXR:
Differential Diagnosis Algorithm ... Respiratory Distress Syndrome ... Respiratory Distress Syndrome ... #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
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
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
Kawasaki Disease (Mucocutaneous Lymph Node Syndrome) An rare systemic acute febrile vasculitic syndrome. Aetiology unknown. Affects
Mucocutaneous Lymph Node Syndrome ... febrile vasculitic syndrome ... Disease #Features #Signs ... #Symptoms #Diagnosis ... #Peds #Pediatrics
Pediatric Inflammatory Multisystem Syndrome Temporally associated with SARS-CoV-2 infection (PIMS-TS) #PIMSTS #Pediatrics #Inflammatory #Multisystem #Syndrome #Peds #Signs
Pediatric Inflammatory ... Multisystem Syndrome ... PIMS-TS) #PIMSTS #Pediatrics ... #Multisystem #Syndrome ... #Peds #Signs #Symptoms
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... =>Prader-Willi Syndrome ... Signs/Symptoms ... pathophysiology #peds ... #pediatrics
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
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
Newborn Infant - ... is also a late sign ... #Newborn #Infant ... #Examination #Peds ... #Pediatrics #Diagnosis
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