4 results
pathophysiology 21hydroxylasedeficiency alternating canuliculitis dacrolith dysfunction endocrinology enophthalmos exophthalmos expression eyelid genetics granule otitismedia physicalexam proptosis respiratory variation
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 ... endocrinology #peds ... #pediatrics
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
Pathogenesis and Clinical ... Bilateral AOM mostly ... pathophysiology #diagnosis ... #symptoms #signs ... #peds #pediatrics
Intermittent Bilateral Exophthalmos (Alternating Exophthalmos and Enophthalmos) on Physical Exam Observing this patient in silence for a
Patient underwent a diagnostic ... symptoms which ... The cause of this ... #clinical #video ... #ophthalmology
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 Dacrolith Eyelid Expression Chronic canuliculitis typically presents with recurrent unilateral epiphora and a pouting punctum. Other
Other signs include ... Common causes are ... this patient, her symptoms ... #Dysfunction #clinical ... #video #ophthalmology
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