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causes differential pathophysiology algorithm genetics 21hydroxylasedeficiency 21ohd alzheimersdisease apgar assessment complications dementia disease endocrinology examination features floppy hypotonic infancy inflammatory
Newborn Assessment - APGAR Score Assessment of newborn vital signs following labor via a 10-point scale evaluated
Newborn Assessment ... vital signs following ... there is increased risk ... #Diagnosis #Peds ... #Pediatrics #APGAR
Causes of Sudden Unexpected Death in Infancy (SUDI) - Differential Diagnosis Algorithm Congenital Anomaly / Disorder: •
- Differential Diagnosis ... Death Syndrome ... 80% of SUDI • Risk ... #Causes #Peds # ... Pediatrics
Kawasaki Disease (Mucocutaneous Lymph Node Syndrome) An rare systemic acute febrile vasculitic syndrome. Aetiology unknown. Affects
Early diagnosis ... immunoglobulin reduces the risk ... Disease #Features #Signs ... #Symptoms #Diagnosis ... #Peds #Pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome ... Signs/Symptoms ... delayed puberty -> Infertility ... pathophysiology #peds ... #pediatrics
Pediatric Inflammatory Multisystem Syndrome Temporally associated with SARS-CoV-2 infection (PIMS-TS) #PIMSTS #Pediatrics #Inflammatory #Multisystem #Syndrome #Peds #Signs
Pediatric Inflammatory ... Multisystem Syndrome ... PIMS-TS) #PIMSTS #Pediatrics ... #Peds #Signs #Symptoms ... #Diagnosis
Alzheimer’s Disease: Pathogenesis and Clinical Findings Risk factor for Late Onset Alzheimer's (99% of cases): - Increasing
Clinical Findings Risk ... mutations - Down syndrome ... pathophysiology #geriatrics ... #diagnosis #signs ... #symptoms
Preterm Infant Complications - Differential Diagnosis Respiratory: • Transient Tachypnea of the Newborn (TTN) • Respiratory Distress
- Differential Diagnosis ... Tachypnea of the Newborn ... Respiratory Distress Syndrome ... #Causes #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 ... endocrinology #peds ... #pediatrics
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic Infant ... (Floppy Newborn ... Other Congenital Syndromes ... Algorithm #Causes #Peds ... #Pediatrics
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
Newborn Infant - ... is also a late sign ... #Newborn #Infant ... #Examination #Peds ... #Pediatrics #Diagnosis
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