10 results
signs diagnosis disease infant kawasaki pathophysiology timeline 21hydroxylasedeficiency 21ohd assessment cirrhosis clinical dehydration elbow endocrinology evaluation examination febrile fever findings
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Syndrome Signs ... /Symptoms/Complications ... PraderWilli #Syndrome #genetics ... pathophysiology #peds ... #pediatrics
The Febrile Child - some diagnostic clues to evaluating the febrile child. #Febrile #Fever #Evaluation #Assessment #Signs
Evaluation #Assessment #Signs ... #Symptoms #PhysicalExam ... #Diagnosis #Peds ... #Pediatrics
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... Extremities #PhysicalExam ... #Signs #Symptoms ... #Dehydration #Peds ... #Pediatrics
Clinical Features and Complications of Measles Rash: Spreads downwards, from behind the ears to the whole Of the
Clinical Features ... Kopliks KoplikSpots #Peds ... #Pediatrics #Timeline ... #Signs #Symptoms
Kawasaki Disease (Mucocutaneous Lymph Node Syndrome) An rare systemic acute febrile vasculitic syndrome. Aetiology unknown. Affects
Kawasaki #Disease #Features ... #Signs #Symptoms ... #Diagnosis #Peds ... #Pediatrics
Clinical features of Liver Disease in Children #Cirrhosis #LiverFailure #Signs #Symptoms #PhysicalExam #Findings #Diagnosis #Peds #Pediatrics #Hepatology **
Clinical features ... #LiverFailure #Signs ... #Symptoms #PhysicalExam ... Findings #Diagnosis #Peds ... #Pediatrics #Hepatology
Pediatric Elbow Injuries - Elbow Xrays Check the fat pads on the lateral projection: 1. A displaced anterior
Pediatric Elbow ... fat pad (sail sign ... A line drawn along ... Draw the RC line ... Xrays #Radiology #peds
Kawasaki Disease - Timeline of Clinical Features and Complications - Fever >5 days - 4
Timeline of Clinical Features ... of the 5 other features ... Disease #Timeline #Features ... #Signs #Symptoms ... #Peds #Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... pathophysiology #genetics ... endocrinology #peds ... #pediatrics
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
is also a late sign ... paediatrician or geneticist ... Newborn #Infant #PhysicalExam ... #Examination #Peds ... #Pediatrics #Diagnosis
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