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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 ... a scrotum #21HydroxylaseDeficiency ... #21OHD #pathophysiology ... endocrinology #peds
This chart shows the percentiles of weight for boys from birth to 36 months.
How to read
from birth to 36 ... shows ages, from birth ... that at birth 95% ... #Diagnosis #Peds ... #Males #Birth #
This chart shows the percentiles of length (height) for boys from birth to 36 months.
How to
from birth to 36 ... shows ages, from birth ... that at birth 95% ... #Diagnosis #Peds ... #Males #Birth #
This chart shows the patterns of height (length) and weight for children from birth to 36
children from birth ... that at birth 95% ... of boys are less ... #Diagnosis #Peds ... #Males #Birth #