Meningohydroencephalocoele Explained
| Meningohydroencephalocoele |
| Field: | neurology |
Meningohydroencephalocoele (AmE: meningohydroencephalocele) is a form of meningocele (AmE)—a developmental abnormality of the central nervous system.
Like meningocoele, meningohydroencephalocoele is caused by defects in bone ossification; in particular, the intramembranous ossification related to the closure of infantile fontanelles. It refers to the protrusion of the meninges between the un-fused bones, to lie subcutaneously.
- Meningocoele - refers to herniation of meninges.
- Meningoencephalocoele refers to the condition if brain tissue is included with the meninges in the herniation.
- Meningohydroencephalocoele refers to the condition including meninges, brain tissue and part of the ventricular system in the herniation.
Encephalocoele defects occur in approximately 1 in 2000 live births.[1]
External links
Notes and References
- Book: Moore, Keith L. . The Developing Human E-Book: Clinically Oriented Embryology . Persaud . T. V. N. . Torchia . Mark G. . 2015 . Elsevier Health Sciences . 9780323313483 . 403 . en.
