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diagnosis management radiology treatment 21hydroxylasedeficiency 21ohd algorithm cardiomyopathy chf classification criticalcare ctchest cxr cystic dementia endocrinology foamed foot freiberg geriatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #genetics #endocrinology ... #peds #pediatrics
Major neurocognitive disorders (MNCD): Diagnosis and workup 1) Clinical diagnosis Cognitive impairment + loss of autonomy 2)
workup 1) Clinical ... MRI, iADL scale, ... (parkinsonian signs ... hyperorality, - 25% genetic ... MNCD #Dementia #Differential
Freiberg Infraction - MSK Radiology Imaging Findings: • Sclerosis of the 2nd MT head with flattening of
Case description ... for secondary signs ... • Unstable 2nd ... Differential diagnosis ... #mri #clinical
Peripartum Cardiomyopathy - Summary 1. Definition • Towards the end of pregnancy to 5 months postpartum
exclude other causes ... Differential Diagnosis ... Genetic predisposition ... during Delivery • Stable ... diagnosis #management #cardiology
It is important to recognize Acute Decompensated Heart Failure (ADHF) as more than just simply a
Signs of poor perfusion ... Signs of congestion ... the determined cause ... #diagnosis #differential ... algorithm #management #cardiology
On the left a chest film of a 19 year old patient with Langerhans cell histiocytosis. The
this pattern was caused ... This is late stage ... most challenging differential ... the central dot sign ... #Clinical #Radiology
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