Parietal foramina

MONDO:0018953

Enlarged parietal foramina (EPF) is a developmental defect, characterized by variable intramembranous ossification defects of the parietal bones, which is either asymptomatic, symptomatic (headaches, nausea, vomiting, intellectual disability) or associated with other pathologies.

Also known as: catlin marks, enlarged parietal foramina, fenestrae parietales symmetricae, foramina parietalia permagna, hereditary cranium bifidum, parietal foramina, symmetric parietal foramina

1 clinical trial for this condition and its sub-types, 0 tagged with Parietal foramina itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Hereditary neurological disease (5772) ↑ Skeletal dysplasia (660) ↑ Neural tube defect (23)

Sub-types of Parietal foramina

Including sub-types (1) Tagged with Parietal foramina (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.