12 results
pediatrics diagnosis assessment differential newborn physicalexam algorithm 21hydroxylasedeficiency 21ohd apgar asthma atopic chronic clinical disease eczema endocrinology epiglottitis evaluation examination
Newborn Assessment - APGAR Score Assessment of newborn vital signs following labor via a 10-point scale evaluated
Newborn Assessment ... Assessment of newborn ... vital signs following ... #Diagnosis #Peds ... #Pediatrics #APGAR
Neonatal Infant Pain Scale (NIPS) For infants less than one year of age, the Neonatal Infant Pain
Pain Scale (NIPS) uses ... A score of 5 or ... #Diagnosis #Peds ... #Pediatrics #PainScale ... #NIPS #Assessment
The Febrile Child - some diagnostic clues to evaluating the febrile child. #Febrile #Fever #Evaluation #Assessment #Signs
some diagnostic clues ... Fever #Evaluation #Assessment ... #Signs #Symptoms ... PhysicalExam #Diagnosis #Peds ... #Pediatrics
The infant with tachypnea or wheeze - Clinical Conditions to Consider - Bronchiolitis - Pneumonia
The infant with ... disorder - Other causes ... #Diagnosis #Peds ... #Pediatrics #Infant ... #Differential #Assessment
Epiglottitis - Swollen inflamed epiglottis Clinical (Rapid onset) • Fever • Sore throat
• Fever • Sore ... #Epiglottitis #Signs ... #Causes #Diagnosis ... #Differential #Peds ... #Pediatrics
Assessment of the Child with Chronic Asthma Are there other allergic disorders? - Allergic rhinitis - Eczema,
Assessment of the ... Other causes should ... Chronic #Asthma #Assessment ... #diagnosis #peds ... #pediatrics #primarycare
Assessment of the Child with Eczema Distribution of atopic eczema - The distribution of eczema tends to
Assessment of the ... In infants, the ... Causes of exacerbation ... #Eczema #Assessment ... #primarycare #peds
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
Infants ≤6 months ... effusion, or z scores ... clinical and lab signs ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... deficiencies present in infants ... Signs/Symptoms/Complications ... 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 ... always needs urgent assessment ... are observed for signs ... #Examination #Peds
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