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21hydroxylasedeficiency ctchest cystic endocrinology genetics histiocytosis langerhanscellhistiocytosis lch peds radiology radiologyassistant
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... , vomiting • Late ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology
On the left a chest film of a 19 year old patient with Langerhans cell histiocytosis. The
This is late stage ... most challenging differential ... the central dot sign ... #Clinical #Radiology ... #CXR #CTChest #
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