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bruising cyanosis facial meconium perioral 21hydroxylasedeficiency 21ohd brudzinskis cord endocrinology genetics large lga meningitis physicalexam sign stain staining ucsdh umbilical
Acrocyanosis: Bluish discoloration of the hands and feet commonly seen in newborns. Charlie Goldberg, M.D. - UCSD
Acrocyanosis: Bluish ... Images #Clinical ... #Peds #Pediatrics ... #Acrocyanosis # ... Newborn #Photo #
Acrocyanosis- Note the contrast between the feet and the color of the right leg. #clinical #photo
Acrocyanosis- Note ... #clinical #photo ... #newborn #peds ... #pediatrics #acrocyanosis
Acrocyanosis- Here again, the cyanosis of the feet is apparent in comparison to the parent's hand
Acrocyanosis- Here ... #clinical #photo ... #newborn #peds ... #pediatrics #acrocyanosis
perioral cyanosis- A blue color around the lips and philtrum is a relatively common finding shortly
This is part of acrocyanosis ... #clinical #photo ... #peds #pediatrics ... #newborn #perioral ... #cyanosis #acrocyanosis
Acrocyanosis- Shortly after birth, cyanosis of the hands, feet, and perioral area are common findings. In
Acrocyanosis- Shortly ... In this photo, notice ... #clinical #photo ... #newborn #peds ... #pediatrics #acrocyanosis
Acrocyanosis- As this infant is transitioning, the blue color on the feet is starting to resolve
Acrocyanosis- As ... #clinical #photo ... #peds #pediatrics ... #newborn #acrocyanosis
This is another example of facial bruising. Here again the face appears to be cyanotic (including
bruising in a newborn ... facial #bruising #newborn ... #peds #pediatrics ... #clinical #photo
Perioral cyanosis- Another newborn with perioral cyanosis clearly demonstrates that although the philtrum and upper chin
cyanosis- Another newborn ... perioral #cyanosis #clinical ... #photo #peds #pediatrics ... #newborn
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
While the pathophysiology ... meningitis, it has low sensitivity ... Sign #Meningitis #Clinical ... #PhysicalExam #Pediatrics ... #Peds
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 21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... , vomiting • Late ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics
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