From the case: Currarino syndrome

Sagittal T2
Modality: MRI (T2)

- “ Family history of Currarino syndrome. This individual is MNXI gene mutation positive.  Case courtesy do A.Prof Damien Stella.  ”

Used in the following article:

  • Currarino syndrome - “ The Currarino syndrome is a complex condition variably comprised of characteristic congenital anomalies of the sacrum, anorectum and presacral sof...”

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