Pathologist Pediatric In-Patient Genetic Stewardship
Conclusions: Approximately 40% of the sendout genetic testing costs were reduced with prior test review. Deferment, alternative laboratories, and sponsored tests contributed to cost savings. Efficiency of diagnostic inpatient genetic testing was approximately 20%.PMID:37787107 | DOI:10.1080/15513815.2023.2263790 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - October 3, 2023 Category: Pathology Authors: Randall Craver Source Type: research
The Placenta and Neonatal Encephalopathy with a Focus on Hypoxic-Ischemic Encephalopathy
Conclusion: No apparent consensus exists on whether it is fetal inflammation with the release of cytokines or chronic maternal and/or fetal vascular malperfusion is responsible for HIE with a lowering of the threshold for hypoxic ischemia. The counter argument is that HIE occurs solely as an intrapartum event. Additional investigation is necessary.PMID:37766587 | DOI:10.1080/15513815.2023.2261051 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - September 28, 2023 Category: Pathology Authors: Louis P Dehner Source Type: research
Molecular Prevalence and Genotype Distribution of Human Adenovirus in Iranian Children with Gastroenteritis
CONCLUSION: HAdV was most common in the 24-60-month-old children. Of the samples sequenced, we found only types 2 and 41. Our results show that in addition to HAdV types 40 and 41, HAdV type 2 may also play a role in causing gastroenteritis in children.PMID:37766589 | DOI:10.1080/15513815.2023.2262576 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - September 28, 2023 Category: Pathology Authors: Abdulhussain Kadhim Jwaziri Mohammad Hadi Karbalaie Niya Pegah Khales Atefeh Kachooei Milad Sabaei Soheil Rahmani Fard Ahmad Tavakoli Source Type: research
The Placenta and Neonatal Encephalopathy with a Focus on Hypoxic-Ischemic Encephalopathy
Conclusion: No apparent consensus exists on whether it is fetal inflammation with the release of cytokines or chronic maternal and/or fetal vascular malperfusion is responsible for HIE with a lowering of the threshold for hypoxic ischemia. The counter argument is that HIE occurs solely as an intrapartum event. Additional investigation is necessary.PMID:37766587 | DOI:10.1080/15513815.2023.2261051 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - September 28, 2023 Category: Pathology Authors: Louis P Dehner Source Type: research
Molecular Prevalence and Genotype Distribution of Human Adenovirus in Iranian Children with Gastroenteritis
CONCLUSION: HAdV was most common in the 24-60-month-old children. Of the samples sequenced, we found only types 2 and 41. Our results show that in addition to HAdV types 40 and 41, HAdV type 2 may also play a role in causing gastroenteritis in children.PMID:37766589 | DOI:10.1080/15513815.2023.2262576 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - September 28, 2023 Category: Pathology Authors: Abdulhussain Kadhim Jwaziri Mohammad Hadi Karbalaie Niya Pegah Khales Atefeh Kachooei Milad Sabaei Soheil Rahmani Fard Ahmad Tavakoli Source Type: research
The Placenta and Neonatal Encephalopathy with a Focus on Hypoxic-Ischemic Encephalopathy
Conclusion: No apparent consensus exists on whether it is fetal inflammation with the release of cytokines or chronic maternal and/or fetal vascular malperfusion is responsible for HIE with a lowering of the threshold for hypoxic ischemia. The counter argument is that HIE occurs solely as an intrapartum event. Additional investigation is necessary.PMID:37766587 | DOI:10.1080/15513815.2023.2261051 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - September 28, 2023 Category: Pathology Authors: Louis P Dehner Source Type: research
Molecular Prevalence and Genotype Distribution of Human Adenovirus in Iranian Children with Gastroenteritis
CONCLUSION: HAdV was most common in the 24-60-month-old children. Of the samples sequenced, we found only types 2 and 41. Our results show that in addition to HAdV types 40 and 41, HAdV type 2 may also play a role in causing gastroenteritis in children.PMID:37766589 | DOI:10.1080/15513815.2023.2262576 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - September 28, 2023 Category: Pathology Authors: Abdulhussain Kadhim Jwaziri Mohammad Hadi Karbalaie Niya Pegah Khales Atefeh Kachooei Milad Sabaei Soheil Rahmani Fard Ahmad Tavakoli Source Type: research
The Placenta and Neonatal Encephalopathy with a Focus on Hypoxic-Ischemic Encephalopathy
Conclusion: No apparent consensus exists on whether it is fetal inflammation with the release of cytokines or chronic maternal and/or fetal vascular malperfusion is responsible for HIE with a lowering of the threshold for hypoxic ischemia. The counter argument is that HIE occurs solely as an intrapartum event. Additional investigation is necessary.PMID:37766587 | DOI:10.1080/15513815.2023.2261051 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - September 28, 2023 Category: Pathology Authors: Louis P Dehner Source Type: research
Molecular Prevalence and Genotype Distribution of Human Adenovirus in Iranian Children with Gastroenteritis
CONCLUSION: HAdV was most common in the 24-60-month-old children. Of the samples sequenced, we found only types 2 and 41. Our results show that in addition to HAdV types 40 and 41, HAdV type 2 may also play a role in causing gastroenteritis in children.PMID:37766589 | DOI:10.1080/15513815.2023.2262576 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - September 28, 2023 Category: Pathology Authors: Abdulhussain Kadhim Jwaziri Mohammad Hadi Karbalaie Niya Pegah Khales Atefeh Kachooei Milad Sabaei Soheil Rahmani Fard Ahmad Tavakoli Source Type: research
Prenatal Array-CGH Detection of 3q26.32q26.33 Interstitial Deletion Encompassing the < em > SOX2 < /em > Gene: Ultrasound, Pathological, and Cytogenetic Findings
Conclusion: The human SOX2 gene (OMIM #184429) is located on chromosome 3 at position q26.3-27 and encodes a transcription factor involved in the development of the central and peripheral nervous systems, retina, and lung. In our case, the combination of cerebral, retinal, and pulmonary anomalies, not previously described, are consistent with SOX2 haploinsufficiency due to chromosomal deletion.PMID:37747279 | DOI:10.1080/15513815.2023.2261043 (Source: Fetal and Pediatric Pathology)
Source: Fetal and Pediatric Pathology - September 25, 2023 Category: Pathology Authors: Maria Paola Bonasoni Giuseppina Comitini Mariangela Pati Veronica Bizzarri Veronica Barbieri Maria Marinelli Stefano Giuseppe Caraffi Roberta Zuntini Marzia Pollazzon Andrea Palicelli Livia Garavelli Source Type: research
