1033 results
Inherited Colorectal Cancer (CRS) Syndromes
Adenomatous Polyposis Syndromes:
 • Familial Adenomatous Polyposis (FAP), Attenuated FAP (AFAP), MUTYH
Colorectal Cancer (CRS) Syndromes ... Adenomatous Polyposis Syndromes ... Urinary → Lynch Syndrome ... Autosomal Dominant, 1 ... Peutz-Jeghers Syndrome
Ramsay Hunt Syndrome - Herpes Zoster Oticus 
Triad:
1. Ipsilateral facial paralysis 
2. Ear pain 
3. Vesicles
Ramsay Hunt Syndrome ... Oticus Triad: 1. ... Guillain-Barré syndrome ... • Stroke syndromes ... #RamsayHunt #Syndrome
Functional Dyspepsia Syndromes - Epigastric Pain Syndrome (EPS) and Postprandial Distress Syndrome (PDS)
Epigastric Pain Syndrome (EPS):
≥
Epigastric Pain Syndrome ... (EPS): ≥ 1 of: ... (PDS) ≥1 of: ... Postprandial fullness (≥1 ... Early satiety (≥1
Nephritic vs Nephrotic Syndrome

Step 1: If the patient has hematuria and/or proteinuria, think about nephrotic/nephritic syndromes.
Step
Nephritic vs Nephrotic Syndrome ... Step 1: If the ... nephrotic/nephritic syndromes ... Nephritic #Nephrotic #Syndrome
Recurrent Polymorphic VT/Torsades de Pointes - Management Algorithm
Drugs that prolong QT interval:
 • Class 1a (quinidine,
Macrolides and quinolones ... Congenital long QT Syndrome ... after load: 0.5-1 ... Pediatric: 0.1-1 ... evidence • Load: 1-
Antibiotic Classification by Mechanism of Action

Cell Wall Synthesis: 
Penicillins 
Cephalosporins 
Carbapenems 
Monobactams 
Beta-lactamase inhibitors
Glycopeptides 

 Protein
Fluorquinolones Quinolones ... Recommended Text: Clinical
Marfan Syndrome - Signs and Symptoms

- Caused by mutations in the fibrillin-1 (FBN1) Gene (chromosome 15)
-
Marfan Syndrome ... the fibrillin-1 ... Dominant #Marfans #Syndrome
Brugada syndrome Types 1, 2 and 3

There are three types of ECG presentations, referred to as
Brugada syndrome ... Types 1, 2 and ... referred to as type 1, ... diagnostic) is type 1 ... Brugada syndrome
BEE Syndromes - Non-inflammatory Causes

Immune-mediated conditions affecting the Brain, Eye, and Ear

Visual or auditory symptoms in
BEE Syndromes - ... repair exonuclease 1 ... optic atrophy-1 ... recessive—Usher syndrome ... MRI lesions and clinical
Hepatopulmonary Syndrome (HPS) 

HPS-differential diagnosis:
1. Pulmonary vasculature
2. Diseases of the lung parenchyma
3. Pleura and diaphragm

HPS-diagnosis:
1. Patients
Hepatopulmonary Syndrome ... HPS-differential diagnosis: 1. ... HPS-diagnosis: 1. ... Hepatopulmonary #Syndrome