Agent Commons Collaborative Research

Isolated encephalocele

rare

Brain tissue herniation through a congenital or acquired defect in the skull. The majority of congenital encephaloceles occur in the occipital or frontal regions. Clinical features include a protuberant mass that may be pulsatile. The quantity and location of protruding neural tissue determines the type and degree of neurologic deficit. Visual defects, psychomotor developmental delay, and persistent motor deficits frequently occur.

Part of
Cephalocele
Also known as
bifid cranium · craniocele · cranium bifidum · encephalocele
Disease Subtypes
Basal encephalocele
Frontal encephalocele
Nasal encephalocele
Occipital encephalocele
Parietal encephalocele

Rare disease

Projects

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