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pediatrics diagnosis acrocyanosis assessment differential meconium physicalexam 21hydroxylasedeficiency 21ohd algorithm bruising cyanosis endocrinology examination facial floppy genetics hand hypotonic infants
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic ... Infant (Floppy ... Newborn) - Differential ... • Central Core ... #Peds #Pediatrics
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 infant with tachypnea or wheeze - Clinical Conditions to Consider - Bronchiolitis - Pneumonia
tachypnea or wheeze - Clinical ... disorder - Other causes ... #Diagnosis #Peds ... #Pediatrics #Infant ... #Differential #Assessment
perioral cyanosis- A blue color around the lips and philtrum is a relatively common finding shortly
The skin in this infant ... #clinical #photo ... #peds #pediatrics ... #newborn #perioral
...this infant is large for gestational age (LGA) with a birth weight of about 9 1/2
the umbilical cord ... though mild in this photo ... #clinical #newborn ... #LGA #large #peds ... #pediatrics
Meconium stained umbilical cord- This cord is about 7 hours old at the time of the
the time of the photo ... effect on the infant ... #clinical #photo ... #newborn #peds ... #pediatrics #meconium
Facial bruising- Marked bruising of the face can occur during delivery. It is more common when
a tight nuchal cord ... When the infant ... #peds #pediatrics ... #clinical #photo ... facial #bruising #newborn
Meconium staining- Evidence of meconium staining in utero may be a clue to an infant who
be a clue to an infant ... the umbilical cord ... #clinical #photo ... #newborn #peds ... meconium #staining #pediatrics
Acrocyanosis- As this infant is transitioning, the blue color on the feet is starting to resolve
Acrocyanosis- As this infant ... #clinical #photo ... #peds #pediatrics ... #newborn #acrocyanosis
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... deficiencies present in infants ... endocrinology #peds ... #pediatrics
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