66 results
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
various types of congenital ... comparison #treatment #Peds ... Endocrinology #Adrenal #pathophysiology
Congenital Nystagmus on Physical Exam
These abnormal eye movements were found in a patient with albinism. What
Congenital Nystagmus ... Diagnosis: Congenital ... achromatopsia, & formal ophthalmology ... PhysicalExam #ocular #clinical ... video #neurology #ophthalmology
Characteristic eye movements found in congenital nystagmus

Video by Kathleen B. Digre, M.D. - Moran Eye Center

#Congenital
movements found in congenital ... Eye Center #Congenital ... #Nystagmus #Ophthalmology ... #Neurology #Clinical
Central Retinal Vein Occlusion (CRVO): Pathogenesis and clinical findings

#CentralRetinalVein #Occlusion #CRVO #pathophysiology #ophthalmology #diagnosis #signs #symptoms
Pathogenesis and clinical ... Occlusion #CRVO #pathophysiology ... #ophthalmology
Aortic Stenosis & Bicuspid Aortic Valve (AS)
 • Introduction & Pathophysiology
 • Classifications
 • Epidemiology
 •
Introduction & Pathophysiology ... Epidemiology • Clinical ... AorticValve #cardiology #peds
Rubella (German Measles)
Rubella, also called German measles, often presents with a mild febrile illness with a
Congenital infection ... defects and death) Clinical ... lymphadenopathy #Rubella #Peds
Undifferentiated critical congenital heart disease: Patterns of Presentation 
Pink baby:
 • Presents at 1-6 mo
Undifferentiated critical ... congenital heart ... annyoungMD #Congenital ... Blue #Gray #Baby #Peds
Marcus-Gunn Jaw Winking Ptosis

Marcus Gunn Jaw Winking Ptosis is the most common form of congenital neurogenic
common form of congenital ... Winking #Ptosis #clinical ... video #neurology #ophthalmology
Central Retinal Vein Occlusion (CRVO)
 - Pathophysiology not fully understood; possibly due to thrombus located in
Occlusion (CRVO) - Pathophysiology ... retinopathy) #Clinical ... #Ophthalmology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... also known as "congenital ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds