Our son 12 years, has this diagnosis. He has a white matter change in the midline of his cerebellum shown on MRI which has remained essentialy the same over 3 years. Because he has been tested for all other known leukodystrophies and all have come back negative his Dr gave him this label for want of a name. It isn't a known entity yet . Hope this is of some help
Canavan disease in Ashkenazi Jews, or globoid cell leukodystrophy (GLD) and metachromatic leukodystrophy (MLD) in Scandinavians.
It is the cerebellar vermis.
Einstin
The middle cerebellar peduncle is the thickest of the three cerebellar peduncles. It is the largest and most prominent of the three, connecting the cerebellum to the brainstem and allowing for communication between the cerebellum and other parts of the brain.
purkinje cells
The juvenile form of metachromatic leukodystrophy is characterized by gait disturbances, urinary incontinence, mental deterioration, and emotional difficulties
It's the middle cerebellar peduncle.As for superior cerebellar and inferior cerebellar peduncles, they are both contain afferent and efferent fibres.
It was incorporated in 1982
Superior cerebellar peduncle (it's also the most medial of the 3 peduncles)
I am not sure... Although, I suffer majorly from Hemi-Hyper Trophy. I am 13. It is very hard to deal with. Do you have Leukodystrophy oh Hemi-Hyper Trophy?
All types of leukodystrophy are genetic (present at conception), progressive, and never spontaneously resolve. None of the leukodystrophies can be cured, and effective treatments are limited.
Metachromatic leukodystrophy (MLD) is a rare degenerative neurological disease affecting the fatty covering that acts as an insulator around nerve fibers known as the myelin sheath.