21 results
pediatrics diagnosis clinical percentiles newborn length weight boys cardiology females girls males management hand nejm physicalexam 21hydroxylasedeficiency 21ohd adrenal arteriosus
Tetralogy of Falot on Chest X-Ray Tetralogy of Falot comprises four defects - 1. Ventricular septal defect (VSD) 2.
Falot on Chest X-Ray ... develops after birth ... #Falot #Chest #XRay ... CXR #clinical #radiology ... #peds #pediatrics
...this infant is large for gestational age (LGA) with a birth weight of about 9 1/2
age (LGA) with a birth ... weight of about ... more glycogen at birth ... with high insulin ... newborn #LGA #large #peds
Truncus Arteriosus • Basic Information • Embryology • Associated anomalies • Pathophysiology/Presentation • Pre-operative management •
Classic Chest Xray ... pulmonary vasculature, right ... diagnosis #management #cardiology ... #peds #pediatrics
Plain radiography of the abdomen revealed calcification of both adrenal glands. A homozygous mutation in LIPA
#clincial #peds ... calcifications #infant ... NEJM #Wolmans #radiology ... #xray
This chart shows the patterns of height (length) and weight for children from birth to 36
children from birth ... shows that at birth ... #Diagnosis #Peds ... #Pediatrics #GrowthCharts ... #Infant #Weight
This chart shows the patterns of height (length) and weight for children from birth to 36
children from birth ... shows that at birth ... #Diagnosis #Peds ... #Pediatrics #GrowthCharts ... #Infant #Weight
This chart shows the percentiles of weight for boys from birth to 36 months. How to read
for boys from birth ... shows that at birth ... #Diagnosis #Peds ... #GrowthCharts # ... #Infant #Weight
This chart shows the percentiles of length (height) for girls from birth to 36 months. How to
for girls from birth ... shows that at birth ... #Diagnosis #Peds ... #GrowthCharts # ... #Infant #Length
This chart shows the percentiles of length (height) for boys from birth to 36 months. How to
for boys from birth ... shows that at birth ... #Diagnosis #Peds ... #GrowthCharts # ... #Infant #Length
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
labeled as males at birth ... deficiencies present in infants ... decr feeding, weight ... like a penis at birth ... endocrinology #peds
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