17 results
diagnosis pediatrics differential management neurology causes physicalexam genetics newborn pulmonary symptoms 21hydroxylasedeficiency 21ohd abnormal abnormalities als amyotrophic antenatal aphasia breathing
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
dehydration in an infant ... Decreased level ... urine output Cold ... #PhysicalExam #Signs ... #Dehydration #Peds
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic Infant ... Differential Diagnosis Algorithm ... Nervous System - Decreased ... • Central Core ... #Causes #Peds #
Causes of Pediatric Stridor - Differential Diagnosis Algorithm Present Since Infancy with No Respiratory Distress: • Laryngomalacia Present
Differential Diagnosis Algorithm ... Present Since Infancy ... Present Since Infancy ... Hemangioma • Vocal Cord ... #Causes #Peds #
Pediatric SVT - Management Algorithm Identify SVT: • HR not variable • Abrupt rate changes • Infants:
SVT - Management Algorithm ... rate changes • Infants ... Signs of shock or ... tachycardia #Management #Algorithm ... #peds #Pediatric
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
gestational diabetes algorithm ... #Infant #Diabetic ... OBGYN #Diagnosis #Pathophysiology ... Complications #Peds
Aphasia - Pathophysiology and Clinical Findings Broca's Aphasia - Expressive language impairment: non-Fluent - Sensory speech areas
Aphasia - Pathophysiology ... comprehension (intact ... areas → Errors in word ... deficits #Aphasia #Pathophysiology ... #diagnosis #signs
Hypochloremia - Differential Diagnosis Algorithm Cause - Decreased Intake: • Low salt in diet • Exclusive D5W
Differential Diagnosis Algorithm ... Cause - Decreased ... - Gitelman SIGNS ... acidosis - Cl⁻ decrease ... #Pathophysiology
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 ... Late (shock): cold ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski) Brudzinski's sign is characterized
Brudzinski’s Sign ... Brudzinski's sign ... causes spinal cord ... While the pathophysiology ... PhysicalExam #Pediatrics #Peds
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 Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... , sleep apnea, cor ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
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