14 results
Causes of Apparent Life Threatening Event (ALTE) - Differential Diagnosis Algorithm
Cardiac:
 • Congenital Heart Disease
 •
Causes of Apparent ... Threatening Event (ALTE ... Myocarditis Metabolic ... Neuromuscular • Disorders ... #Causes #Peds #
Short Stature - Differential Diagnosis Algorithm
Normal Variant, Normal Puberty Onset (BA = CA)
 • Familial Short
Differential Diagnosis Algorithm ... Short Stature (Late ... CHF) • Inborn Metabolism ... #endocrinology ... #causes #pediatrics
Crystalline Keratopathy on Slit Lamp Examination

Slit lamp examination demonstrated scattered refractile particles within the anterior stroma.
disorders, amino ... disorders, metabolic ... and iatrogenic causes ... #Keratopathy #clinical ... #video #physicalexam
Acute Fatty Liver of Pregnancy (AFLP)
Pathophysiology:
 • Defect in fetal free fatty acid metabolism products →
Pregnancy (AFLP) Pathophysiology ... free fatty acid metabolism ... Intermediate fatty acid metabolism ... = nonspecific (nausea ... Findings: • ↑AST/ALT
Diabetic Ketoacidosis (DKA) - Pathogenesis and Clinical Findings
 • Note: in DKA, body K+ is lost
Pathogenesis and Clinical ... out of cells may cause ... Due to neuronal metabolism ... DiabeticKetoacidosis #DKA #pathophysiology ... #endocrinology
Causes of Secondary Hypertension - Workup and Differential Diagnosis
Approach (when evaluation should be done):
1. Severe or
with electrolyte disorders ... hypokalemia and metabolic ... 109 mm Hg) with clinical ... Vasculitis • Endocrinologic ... Neurologic disorders
Refeeding Syndrome Overview

What Is It?
	• Electrolyte/fluid shifts caused by initiation of nutrition in severely malnourished patient.
from hormonal and metabolic ... changes and may cause ... severe clinical ... deficiency (thiamine) Late ... Differential #Diagnosis #Pathophysiology
Pisa Syndrome (pleurothotonus) on Physical Exam
A tonic flexion of the trunk of the body to one
Caused commonly ... neurodegenerative disorders ... Pathophysiology: ... #PhysicalExam #clinical ... neurology #posture #video
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 ... , vomiting • Late ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
Hemichorea-Hemiballismus on Neurological Examination - Movement Disorders

This case was seen in thyrotoxicosis.

#Hemichorea #Hemiballismus #clinical #video #neurology
Examination - Movement Disorders ... This case was ... Hemiballismus #clinical ... #video #neurology ... thyrotoxicosis #endocrinology