24
Sep
Currarino syndrome 7q36 deletion
0 Comment
The paper expands upon the variable expressivity of Currarino syndrome (CS), a rare genetic disorder characterized by a triad of anorectal malformations, sacral bony defects, and presence of a presacral mass, that is caused by variants of or chromosomal arrangements involving MNX1, mapped to 7q36. Currarino syndrome (CS) is a... Read More
