52 results
diagnosis symptoms pediatrics differential management ophthalmology msk syndrome causes hyperthyroidism kawasaki neurology physicalexam algorithm genetics hepatology hypertension mooddisorders pituitary pneumonia
Clinical Examination in Endocrine Diseases #Endocrinology #PhysicalExam #Diagnosis #Signs
Clinical Examination ... in Endocrine Diseases ... #Endocrinology ... PhysicalExam #Diagnosis #Signs
Primary hypoadrenalism (Addison’s disease) – symptoms, signs #Diagnosis #Hypoadrenalism #Addisons #Disease #Hypoadrenalism #Signs #Symptoms ** GrepMed Recommended Text:
hypoadrenalism (Addison’s disease ... ) – symptoms, signs ... Hypoadrenalism #Signs ... Greenspan's Basic and Clinical ... Endocrinology -
Graves’ Disease: Pathogenesis and Clinical Findings B & T lymphocyte mediated autoimmunity attack TSH receptor -> Continuous
Graves’ Disease: ... Pathogenesis and Clinical ... GravesDisease #pathophysiology ... #endocin #endocrinology ... #symptoms #signs
Thyroid Eye Signs Lid Signs Dalrymple’s Sign: Lid Retraction. Von
Thyroid Eye Signs ... Dalrymple’s Sign ... : Lid lag of the ... #EPONYMS #ENDOCRINOLOGY ... OPHTHALMOLOGY #clinical
Primary Hyperthyroidism - Pathogenesis and Clinical Findings Note: Although rare, gestational diseases can lead to thyrotoxicosis due
Pathogenesis and Clinical ... rare, gestational diseases ... Signs/Symptoms: ... Hyperthyroidism #endocrinology ... #pathophysiology
Growth Hormone Excess - Pathogenesis and clinical findings • Acromegaly and gigantism share the same pathophysiology
Pathogenesis and clinical ... Cardiovascular disease ... Overproduction #diagnosis #signs ... #symptoms #endocrinology ... #pathophysiology
Gaucher Disease Pathophsiology • Lysosomal storage disorder • Deficiency of ß-glucocerebrosidase • Accumulation of glucosylceramide in macrophages Diagnosis
Gaucher Disease ... Pathophsiology ... in GBA1 gene Clinical ... #Gauchers #Disease ... #Diagnosis #Signs
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Brudzinski’s Sign ... While the pathophysiology ... despite severe disease ... #Meningitis #Clinical ... PhysicalExam #Pediatrics #Peds
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 Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... • Deletion of critical ... Prader-Willi Syndrome Signs ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
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 ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
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