A Newborn Infant with Congenital Central Hypoventilation Syndrome and Pupillary Abnormalities: A Literature Review
We present a neonate with early onset apnea and bradycardia in the absence of primary cardiorespiratory and central nervous system disorders that eventually required chronic ventilator support starting at 6 hours of life. Molecular testing of paired-like homeobox 2b (PHOX2B) gene mutation confirmed...
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Format: | Book |
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Thieme Medical Publishers, Inc.,
2022-07-01T00:00:00Z.
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Connect to this object online.3rd Floor Main Library
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A1234.567 |
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