Publications by authors named "Scheltema P"

Article Synopsis
  • Intracerebral hemorrhage is uncommon in full-term neonates, with non-genetic factors and genetic variants in COL4A1 and COL4A2 being implicated.
  • A case is reported of a neonate with hemorrhage who has a newly identified intragenic duplication in COL4A2, which may be a risk factor for the condition.
  • Further screening for COL4A1 and COL4A2 duplications is suggested for the diagnosis of unexplained neonatal cerebral hemorrhages to enhance understanding of their potential impact.
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Objective: To propose a staging system for congenital lower urinary tract obstruction (LUTO) capable of predicting the severity of the condition and its prognosis.

Methods: This was a national retrospective study carried out at the eight Academic Hospitals in The Netherlands. We collected prenatal and postnatal data of fetuses at high risk of isolated LUTO that were managed conservatively.

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Objective: To determine outcome of children born with isolated gastroschisis (no extra-gastrointestinal congenital abnormalities).

Study Design: International cohort study and meta-analysis.

Primary Outcome: time to full enteral feeding (TFEF); secondary outcomes: Duration of mechanical ventilation, length of stay (LOS), mortality and differences in outcome between simple and complex gastroschisis (complex; born with bowel atresia, volvulus, perforation or necrosis).

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Objective: To evaluate the performance of a directed non-invasive prenatal testing method of cell-free DNA analysis for fetal trisomy 21 (T21) by shipping the whole blood samples from Europe to a laboratory in the USA.

Methods: A European multicenter prospective, consecutive cohort study was performed enrolling pregnant women from Sweden and the Netherlands. Blood samples were drawn just prior to a planned of invasive diagnostic procedure in a population at increased risk for fetal T21 and then shipped to the USA without any blood processing.

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