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Matthew-Wood Syndrome in Monochorionic, Diamnionic Twins.
Geiculescu, Irina; Saxonhouse, Matthew A; Demmer, Laurie; Sutsko, Ronald; Cosper, Graham; Jones, James E.
Afiliación
  • Geiculescu I; Department of Pediatrics, Levine Children's Hospital, Atrium Healthcare, Charlotte, North Carolina, United States.
  • Saxonhouse MA; Division of Neonatology, Levine Children's Hospital, Atrium Healthcare, Charlotte, North Carolina, United States.
  • Demmer L; Division of Genetics, Levine Children's Hospital, Atrium Healthcare, Charlotte, North Carolina, United States.
  • Sutsko R; Division of Neonatology, Levine Children's Hospital, Atrium Healthcare, Charlotte, North Carolina, United States.
  • Cosper G; Department of Surgery, Atrium Healthcare, Charlotte, North Carolina, United States.
  • Jones JE; Division of Neonatology, Levine Children's Hospital, Atrium Healthcare, Charlotte, North Carolina, United States.
J Pediatr Genet ; 13(2): 123-126, 2024 Jun.
Article en En | MEDLINE | ID: mdl-38721583
ABSTRACT
Matthew-Wood syndrome represents a rare genetic disorder characterized by diaphragmatic defects, pulmonary hypoplasia, micro- or anophthalmia, and cardiac defects. Most cases are lethal with very few infants living beyond a few years of life. Siblings with this diagnosis have been reported but never twins. In this article, we provided a review and discussion of this syndrome following its presentation in monochorionic, diamnionic twin females.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Pediatr Genet Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Pediatr Genet Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos