Matthew-Wood Syndrome in Monochorionic, Diamnionic Twins.
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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MEDLINE
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En
Revista:
J Pediatr Genet
Año:
2024
Tipo del documento:
Article
País de afiliación:
Estados Unidos