Sacrococcygeal dysgenesis association

Abstract excerpt

In the malformation analysis of 445 patients ascertained only for a sacrococcygeal malformation, a new phenotype, the sacrococcygeal dysgenesis association (SDA), was delineated in 34%. In addition, sirenomelia patients were found in 12%, the VATER association in 27%, and 27% could not be classified. Heterogeneity in the patients with sacrococcygeal malformations was identified by the differences found in their...

Topics

Share this publication in a Topic to start or enrich a Post.

• Share to Cleft Lip and Palate Research
• Share to Congenital Ear and Nasal Anomalies
• Share to Congenital gastrointestinal and neural anomalies