Sacral agenesis (also considered as part of the caudal regression syndrome) is a rare and severe sacral developmental abnormality.
On this page:
Epidemiology
In normal pregnancy, the incidence is between 0.005 and 0.1%. However, in fetuses with diabetic mothers, the incidence rises to 0.2%. Of those with the condition, 16-20% have diabetic mothers.
Pathology
Associations
increased frequency of spinal dysraphism
Classification
Sacral agenesis can be categorized into four types 1:
type I: unilateral agenesis localized to sacrum or coccyx
type II: partial agenesis with bilateral defects; the iliac bone articulates with S1, but the distal sacral elements fail to develop
type III: total sacral agenesis; iliac bones articulate with the lowest lumbar element
type IV: total sacral agenesis; iliac bones fuse posteriorly