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acrocyanosis algorithm diagnosis facial meconium 21hydroxylasedeficiency 21ohd cyanosis differential disease endocrinology floppy genetics hand hypotonic incomplete kawasaki large lga pathophysiology
This is another example of facial bruising. Here again the face appears to be cyanotic (including
example of facial bruising ... in a newborn; no ... #newborn #peds ... #pediatrics #clinical ... #photo
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 ... #newborn
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic ... Infant (Floppy ... Newborn) - Differential ... #Floppy #Newborn ... #Peds #Pediatrics
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
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
...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
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
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
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
Infants ≤6 months ... if they have no clinical ... should be given to children ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
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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