Publications by authors named "M Harsono"

Background: Acute kidney injury (AKI) occurs in up to half of infants admitted to the neonatal intensive care unit (NICU) and is associated with increased risks of death and more days of mechanical ventilation, hospitalization, and vasopressor drug support. Our objective was to build a granular relational database to study the impact that AKI has on infants admitted to Level-IV NICUs.

Methods: A relational database was created by linking data from the Children's Hospitals Neonatal Database with AKI-focused data from electronic health records from 9 centers.

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Down syndrome (DS, trisomy 21) with an extra copy of chromosome 21 is one of the most common aneuploidies in humans. Jacobs syndrome or XYY syndrome (trisomy XYY) with an extra copy of sex chromosome Y is a rare sex chromosome trisomy in males. Double aneuploidy (DA) with an extra copy of chromosome 21 and sex chromosome Y is an extremely rare occurrence.

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Article Synopsis
  • A neonate experienced early apnea and bradycardia, requiring chronic ventilator support just 6 hours after birth, without any clear cardiorespiratory or CNS disorders.
  • Genetic testing revealed a mutation in the paired-like homeobox 2b gene, confirming the diagnosis of congenital central hypoventilation syndrome (CCHS), a rare genetic disorder affecting respiratory control.
  • Unusually, the neonate also exhibited signs of ocular autonomic nervous system dysregulation, detected during the first day of life, including persistent mild dilated pupils that had limited responsiveness to light.
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Using the cranial window technique, we investigated acute effects of head cooling on cerebral vascular functions in newborn pigs. Head cooling lowered the rectal and extradural brain temperatures to 34.3 ± 0.

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Perineal groove is a rare benign congenital anomaly with lesion that resembles perforation of mid-perineum or perineal raphe area. Most reported cases of congenital perineal groove presented as an isolated defect in term or early-term singleton female infants. Thus far, there is no reported case of this anomaly in monozygotic twins.

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