b12 peds video sign diagnosis infant clinical symptoms mnemonic algorithm cord 21ohd - GrepMed

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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 ... deficiencies present in infants ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds

Spinal Cord Disorders - Differential Diagnosis Framework

Spinal cord neurological lesion:
Clinical findings:
• Symptoms and signs below

- Differential Diagnosis ... neurological lesion: Clinical ... and signs below ... myelopathy - Vit B12 ... differential #algorithm

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