11 results
Lab patterns seen in Inborn Errors of Metabolism

A table of lab values compiled from UpToDate and
See IEM schema for ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... #Neonatology #Peds ... #NICU #Genetics ... #IEM #Laboratory
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
MetabolicEmergency #Genetics ... #Pathophysiology ... #Diagnosis #Algorithm ... #Neonatology #Peds ... #IEM #NICU #InbornErrors
Algorithm for the evaluation of pediatric cervical spine injuries #Diagnosis #EM #Peds #Trauma #CSpine #Clear #Clearance
Algorithm for the ... evaluation of pediatric ... spine injuries #Diagnosis ... #EM #Peds #Trauma ... Clearance #Decision #Algorithm
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Syndrome Signs/Symptoms ... delayed puberty -> Infertility ... PraderWilli #Syndrome #genetics ... #pathophysiology ... #peds #pediatrics
PATIENT AGE >2 Years - Pediatric Blunt Head Trauma (PECARN Study) #Diagnosis #Management #Peds #EM #Algorithm
AGE >2 Years - Pediatric ... PECARN Study) #Diagnosis ... #Management #Peds ... #EM #Algorithm
Algorithm for the Evaluation of Pediatric Head Trauma (PECARN) - Need for Head CT #Diagnosis #Management
Algorithm for the ... Evaluation of Pediatric ... Need for Head CT #Diagnosis ... #Management #EM ... #Peds #Trauma #
PATIENT AGE <2 Years - Pediatric Blunt Head Trauma (PECARN Study) #Diagnosis #Management #Peds #EM #Algorithm
AGE <2 Years - Pediatric ... PECARN Study) #Diagnosis ... #Management #Peds ... #EM #Algorithm
gestational diabetes algorithm
#Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
gestational diabetes algorithm ... Diabetic #Mother #Pediatrics ... #NICU #OBGYN #Diagnosis ... #Pathophysiology ... Complications #Peds
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... Hirsutism & acne • Infertility ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Evaluation and Management of Pediatric Fever #Diagnosis #Management #EM #Peds #Fever #Workup #Evaluation #Discharge #Admission #Algorithm
Management of Pediatric ... Fever #Diagnosis ... #Management #EM ... #Peds #Fever #Workup ... Discharge #Admission #Algorithm