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pediatrics causes differential algorithm clinical complications diabetes diabetic endocrinology gestational idm management maternal mother neonatology neurology nicu obgyn screening treatment
Infant of a Diabetic Mother - complications - pathophysiology learning schema Information source: UpToDate #Infant #Diabetic #Mother #Pediatrics
Infant of a Diabetic ... #NICU #OBGYN #Diagnosis ... #Pathophysiology ... Complications #Peds ... #Newborn #Obstetrics
gestational diabetes algorithm #Infant #Diabetic #Mother #Pediatrics #Neonatology #IDM #NICU #OBGYN #Diagnosis #Pathophysiology #Maternal #Complications #Peds #Newborn
diabetes algorithm #Infant ... #NICU #OBGYN #Diagnosis ... #Pathophysiology ... Complications #Peds ... #Newborn #Obstetrics
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm Congenital Anomaly / Disorder: •
- Differential Diagnosis ... - Prone Sleeping ... - Sharing a Sleeping ... #Diagnosis #Algorithm ... #Causes #Peds #
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
hyperplasia for the medical ... CongenitalAdrenalHyperplasia #diagnosis ... comparison #treatment #Peds ... Endocrinology #Adrenal #pathophysiology
Urine Color - Differential Diagnosis Red Urine: • Medical conditions: bleeding, porphyria, factitious disorder • Meds: rifampin,
- Differential Diagnosis ... Red Urine: • Medical ... conditions: bleeding ... Pseudomonas • Meds ... #Differential #Diagnosis
Aphasia - Pathophysiology and Clinical Findings Broca's Aphasia - Expressive language impairment: non-Fluent - Sensory speech areas
Aphasia - Pathophysiology ... comprehension (intact ... Fluent (but non-sensical ... deficits #Aphasia #Pathophysiology ... #diagnosis #signs
Preterm Infant Complications - Differential Diagnosis Respiratory: • Transient Tachypnea of the Newborn (TTN) • Respiratory Distress
Preterm Infant Complications ... - Differential Diagnosis ... Tachypnea of the Newborn ... #Differential #Diagnosis ... #Causes #Peds #
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
deficiencies present in infants ... • Early: decr feeding ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds
Alexia Without Agraphia Alexia without agraphia is a disconnection syndrome where patients cannot read but can write.
common cause, leading ... Pathophysiology: ... PCA Infarct (most ... clinical #neurology #diagnosis ... #pathophysiology
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
Newborn Infant - ... When the diagnosis ... #Newborn #Infant ... #Examination #Peds ... #Pediatrics #Diagnosis
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