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Childhood dementia is very often diagnosed late, misdiagnosed, or not diagnosed at all. [9] A correct diagnosis happens, on average, 2 years or more after symptoms become apparent. Additionally, children affected by childhood dementia are often misdiagnosed with: Autism [16] [9] [17] Developmental or intellectual delay [16] [9] ADHD [9] Others [9]
In the human skull, the zygomatic bone (from Ancient Greek: ζῠγόν, romanized: zugón, lit. 'yoke'), also called cheekbone or malar bone, is a paired irregular bone, situated at the upper and lateral part of the face and forming part of the lateral wall and floor of the orbit, of the temporal fossa and the infratemporal fossa.
The zygomatic process forms an "L" in this picture. As a comparison, this is how the skull looks with almost all of the zygomatic process removed. The zygomatic processes (aka. malar) are three processes (protrusions) from other bones of the skull which each articulate with the zygomatic bone. The three processes are: [1]
The term zygoma generally refers to the zygomatic bone, a bone of the human skull that is commonly referred to as the cheekbone or malar bone, but it may also refer to: The zygomatic arch , a structure in the human skull formed primarily by parts of the zygomatic bone and the temporal bone
Pre-dementia or early-stage dementia (stages 1, 2, and 3). In this initial phase, a person can still live independently and may not exhibit obvious memory loss or have any difficulty completing ...
Alzheimer's disease (AD) is a neurodegenerative disease and the most common cause of dementia; it usually occurs in old age. Familial Alzheimer's disease (FAD or EOFAD for early onset) is an inherited and uncommon form of AD. Familial AD usually strikes earlier in life, defined as before the age of 65.
Posterior cortical atrophy (PCA), also called Benson's syndrome, is a rare form of dementia which is considered a visual variant or an atypical variant of Alzheimer's disease (AD). [ 1 ] [ 2 ] [ 3 ] The disease causes atrophy of the posterior part of the cerebral cortex , resulting in the progressive disruption of complex visual processing . [ 4 ]
Previous studies show that genetics can increase a person’s risk of developing Alzheimer’s disease. One genetic variant associated with Alzheimer’s disease progression is presenilin 2 (PSEN2 ...