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Matthew-Wood Syndrome in Monochorionic, Diamnionic Twins
Irina Geiculescu1, Matthew A Saxonhouse2, Laurie Demmer3
1Department of Pediatrics, Levine Children's Hospital, Atrium Healthcare, Charlotte, North Carolina, United States.
Matthew-Wood syndrome, a rare genetic disorder, was identified in monochorionic twin females. This case highlights the syndrome
Area of Science:
- Medical Genetics
- Developmental Biology
- Pediatric Medicine
Background:
- Matthew-Wood syndrome is a rare genetic disorder.
- It is characterized by diaphragmatic defects, pulmonary hypoplasia, microphthalmia/anophthalmia, and cardiac defects.
- Most cases are lethal, with few infants surviving past a few years.
Purpose of the Study:
- To review and discuss Matthew-Wood syndrome.
- To present a unique case of the syndrome in monochorionic, diamnionic twin females.
- To add to the limited understanding of this rare condition.
Main Methods:
- Literature review of Matthew-Wood syndrome.
- Case report of monochorionic, diamnionic twin females with the syndrome.
- Discussion of clinical presentation and implications.
Main Results:
- The syndrome presented in monochorionic, diamnionic twin females.
- This is the first reported case of Matthew-Wood syndrome in twins.
- The review consolidates existing knowledge and presents a novel case.
Conclusions:
- Matthew-Wood syndrome can occur in twins, a previously unreported occurrence.
- This case provides valuable insights into the variability and presentation of the syndrome.
- Further research is needed to understand the genetic and developmental factors in twin presentations.
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