18 results
physicalexam video acrocyanosis algorithm differential genetics meconium pathophysiology primitive reflex 21hydroxylasedeficiency 21ohd apgar babinski bruising causes cries cyanosis dehydration disease
Newborn Assessment - APGAR Score Assessment of newborn vital signs following labor via a 10-point scale evaluated
Newborn Assessment ... of newborn vital ... signs following ... #Diagnosis #Peds ... #Pediatrics #APGAR
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Causes of Hypotonic Infant ... (Floppy Newborn ... - Differential Diagnosis ... Algorithm #Causes #Peds ... #Pediatrics
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... urine output Cold ... #PhysicalExam #Signs ... #Dehydration #Peds ... #Pediatrics
perioral cyanosis- A blue color around the lips and philtrum is a relatively common finding shortly
The skin in this infant ... #clinical #photo ... #peds #pediatrics ... #newborn #perioral
Meconium stained umbilical cord- This cord is about 7 hours old at the time of the
the time of the photo ... effect on the infant ... #clinical #photo ... #newborn #peds ... #pediatrics #meconium
...this infant is large for gestational age (LGA) with a birth weight of about 9 1/2
the umbilical cord ... though mild in this photo ... #clinical #newborn ... #LGA #large #peds ... #pediatrics
The infant with tachypnea or wheeze - Clinical Conditions to Consider - Bronchiolitis - Pneumonia
The infant with ... tachypnea or wheeze - Clinical ... Other causes #Diagnosis ... #Peds #Pediatrics ... #Differential #Assessment
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... delayed puberty -> Infertility ... , sleep apnea, cor ... pathophysiology #peds ... #pediatrics
Facial bruising- Marked bruising of the face can occur during delivery. It is more common when
a tight nuchal cord ... the body, the diagnosis ... #peds #pediatrics ... #clinical #photo ... facial #bruising #newborn
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
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