Congenital portosystemic venous shunt associated with 22q11.2 deletion syndrome: a case report

BACKGROUND: 22q11.2 deletion syndrome (22qDS) is the most common chromosomal microdeletion syndrome and is associated with a high rate of congenital heart disease (CHD) and neurodevelopmental abnormalities. Congenital portosystemic venous shunts (CPSS) are rare developmental abnormalities of the por...

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Detalles Bibliográficos
Autores principales: Ifuku, Toshinobu, Suzuki, Sayo, Nagatomo, Yusaku, Yokoyama, Ryohei, Yamamura, Yoshiko, Nakatani, Keigo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245277/
https://www.ncbi.nlm.nih.gov/pubmed/35768799
http://dx.doi.org/10.1186/s12887-022-03447-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245277/
https://www.ncbi.nlm.nih.gov/pubmed/35768799
http://dx.doi.org/10.1186/s12887-022-03447-3

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