40 results
Infant of a Diabetic Mother - complications - pathophysiology learning schema
Information source: UpToDate

#Infant #Diabetic #Mother #Pediatrics
Infant of a Diabetic ... : UpToDate #Infant ... Diabetic #Mother #Pediatrics ... #NICU #OBGYN #Diagnosis ... #Pathophysiology
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm
Congenital Anomaly / Disorder:
 •
Unexpected Death in Infancy ... - Differential Diagnosis ... Arrhythmia • Neurologic ... #Diagnosis #Algorithm ... #Causes #Peds #Pediatrics
Kernig's Sign in Meningitis

Kernig's sign is present if the patient, in the supine position with the
In this video, the ... infant cries as ... Meningitis #Clinical #Video ... #PhysicalExam #Pediatrics ... #Peds #neurology
Brudzinski's Sign on Physical Exam - Meningitis

#Brudzinskis #Sign #PhysicalExam #clinical #video #neurology #peds #pediatrics #meningitis
Brudzinski's Sign ... #Brudzinskis #Sign ... PhysicalExam #clinical #video ... #neurology #peds ... #pediatrics #meningitis
Scarf Sign (Normal) on Physical Exam

The scarf sign is used to assess developmental age and muscle
Scarf Sign (Normal ... Exam The scarf sign ... The infant's arm ... #clinical #video ... hypotonic #peds #pediatrics
gestational diabetes algorithm
#Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
diabetes algorithm #Infant ... Diabetic #Mother #Pediatrics ... #NICU #OBGYN #Diagnosis ... #Pathophysiology
Gowers' Sign on Physical Exam

Seen in this patient with Duchenne muscular dystrophy (DMD)

#Gowers #Sign #PhysicalExam #neurology
Gowers' Sign on ... DMD) #Gowers #Sign ... #PhysicalExam #neurology ... #clinical #video ... #pediatrics #muscular
Comparison of Causes of Salt-Wasting in Infancy
 - PHA 1
 - PHA 3
 - 21-OH CAH
Salt-Wasting in Infancy ... Salt #Wasting #Infancy ... #differential #diagnosis ... #pediatrics #nephrology
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... delayed puberty -> Infertility ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
deficiencies present in infants ... Signs/Symptoms/Complications ... Hirsutism & acne • Infertility ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics