11 results
acrocyanosis causes diagnosis differential genetics meconium pathophysiology 21hydroxylasedeficiency 21ohd algorithm bruising cyanosis discordant endocrinology facial floppy hypotonic large lga perioral
Preterm Infant Complications - Differential Diagnosis Respiratory: • Transient Tachypnea of the Newborn (TTN) • Respiratory Distress
Preterm Infant Complications ... Tachypnea of the Newborn ... Respiratory Distress Syndrome ... Diagnosis #Causes #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
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Signs/Symptoms/Complications ... , sleep apnea, cor ... pathophysiology #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
Facial bruising- Marked bruising of the face can occur during delivery. It is more common when
a tight nuchal cord ... When the infant ... #peds #pediatrics ... #clinical #photo ... facial #bruising #newborn
Meconium staining- Evidence of meconium staining in utero may be a clue to an infant who
be a clue to an infant ... the umbilical cord ... #clinical #photo ... #newborn #peds ... meconium #staining #pediatrics
Acrocyanosis- As this infant is transitioning, the blue color on the feet is starting to resolve
Acrocyanosis- As this infant ... #clinical #photo ... #peds #pediatrics ... #newborn #acrocyanosis
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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