28 results
Congenital TORCH Infections

Dr. Natalie Marshall @MicrobeNat

#Congenital #Infections #Comparison #Table #pediatrics #diagnosis #symptoms #TORCH
Congenital TORCH ... @MicrobeNat #Congenital ... Infections #Comparison #Table ... #pediatrics #diagnosis ... #symptoms #TORCH
Congenital Infections - Comparison Table:
Infections: Toxoplasma, Rubella, CMV, Treponema, Parvovirus B19, VZV, Herpes, Enterovirus
Manifestations: Anemia, Bony
Congenital Infections ... - Comparison Table ... Thrombocytopenia #Congenital ... #pediatrics #diagnosis ... #symptoms #TORCH
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
schema of the pathophysiology ... the lab values table ... of information: Pediatrics ... , UpToDate #Pediatrics ... #Table #IEM #NICU
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
various types of congenital ... algorithm #causes #pediatrics ... Endocrinology #Adrenal #pathophysiology
Algorithm for the Evaluation and Management of Suspected Congenital Heart Disease in Neonates

Neonates with undiagnosed congenital
Management of Suspected Congenital ... with undiagnosed congenital ... with nonspecific symptoms ... twitter.com/thame #Congenital ... Neonatal #Peds #Pediatrics
Lab patterns seen in Inborn Errors of Metabolism

A table of lab values compiled from UpToDate and
Metabolism A table ... from UpToDate and Pediatrics ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... Neonatology #Peds #Pediatrics ... #Table #NICU #Genetics
Diabetes Insipidus vs Syndrome of Inappropriate ADH (SIADH) - Comparison Table

Diabetes Insipidus - Inadequate ADH
SIADH -
) - Comparison Table ... SIADH #Comparison #Table ... #Pathophysiology ... #Signs #Symptoms
Types of Chronic Urinary Incontinence

Type, Prevalence, Pathophysiology and Symptoms:
 - Stress
 - Urge
 - Mixed
 -
Type, Prevalence, Pathophysiology ... and Symptoms: ... Types #Comparison #Table
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
also known as "congenital ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics
Alzheimer’s Disease: Pathogenesis and Clinical Findings
Risk factor for Late Onset Alzheimer's (99% of cases):
 - Increasing
chromosome 21) Signs / Symptoms ... AlzheimersDisease #Dementia #pathophysiology ... #geriatrics #diagnosis ... #signs #symptoms