7 results
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Females may be labeled ... as males at birth ... deficiencies present in infants ... decr feeding, weight ... endocrinology #peds
This chart shows the patterns of height (length) and weight for children from birth to 36
(length) and weight ... #Diagnosis #Peds ... GrowthCharts #Girls #Females ... #Birth #Infant ... #Weight #Height
This chart shows the patterns of height (length) and weight for children from birth to 36
(length) and weight ... #Diagnosis #Peds ... GrowthCharts #Boys #Males ... #Birth #Infant ... #Weight #Height
This chart shows the percentiles of weight for girls from birth to 36 months.
How to read
for girls from birth ... shows that at birth ... #Diagnosis #Peds ... GrowthCharts #Girls #Females ... #Birth #Infant
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 #Boys #Males ... #Birth #Infant
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 #Girls #Females ... #Birth #Infant
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 #Boys #Males ... #Birth #Infant