Currarino syndrome: a comprehensive genetic review of a rare congenital disorder

BACKGROUND: The triad of a presacral mass, sacral agenesis and an anorectal anomaly constitutes the rare Currarino syndrome (CS), which is caused by dorsal–ventral patterning defects during embryonic development. The major causative CS gene is MNX1, encoding a homeobox protein. MAIN BODY: In the maj...

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Detalles Bibliográficos
Autores principales: Dworschak, Gabriel C., Reutter, Heiko M., Ludwig, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8034116/
https://www.ncbi.nlm.nih.gov/pubmed/33836786
http://dx.doi.org/10.1186/s13023-021-01799-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8034116/
https://www.ncbi.nlm.nih.gov/pubmed/33836786
http://dx.doi.org/10.1186/s13023-021-01799-0

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