22 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
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
various types of congenital ... CongenitalAdrenalHyperplasia #diagnosis ... comparison #treatment #Peds ... Endocrinology #Adrenal #pathophysiology
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
Diabetes Insipidus vs Syndrome of Inappropriate ADH (SIADH) - Comparison Table

Diabetes Insipidus - Inadequate ADH
SIADH -
) - Comparison Table ... SIADH #Comparison #Table ... #Pathophysiology ... #Signs #Symptoms ... #Diagnosis #Endocrinology
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
schema of the pathophysiology ... the lab values table ... #Diagnosis #Algorithm ... #Neonatology #Peds ... #Pediatrics #Table
Lab patterns seen in Inborn Errors of Metabolism

A table of lab values compiled from UpToDate and
Metabolism A table ... additions, for diagnosing ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... #Neonatology #Peds ... #Pediatrics #Table
Types of Chronic Urinary Incontinence

Type, Prevalence, Pathophysiology and Symptoms:
 - Stress
 - Urge
 - Mixed
 -
Type, Prevalence, Pathophysiology ... and Symptoms: ... Functional #Diagnosis ... Types #Comparison #Table
Congenital Long QT Syndrome: Illness Script

Who?
 - Kids or young adults, usually < 30
 - high
Congenital Long ... live births Symptoms ... arrest/death - Symptoms ... specialist #Congenital ... LongQT #Syndrome #Diagnosis
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
Trendelenburg Gait: Pathogenesis and clinical findings

Skeletal Pathology of the Hip
 • Arthritis
 • Congenital hip dysplasia
Arthritis • Congenital ... Trendelenburg #Gait #pathophysiology ... #causes #symptoms ... #signs #diagnosis