Hypo-frontal syndrome is a condition characterized by reduced activity in the frontal lobes of the brain, which can lead to impairments in executive functions such as decision-making, problem-solving, and impulse control. It often manifests in behaviors such as apathy, lack of motivation, and difficulty in planning and organizing tasks. This syndrome can be associated with various neurological disorders, including traumatic brain injury, schizophrenia, and neurodegenerative diseases. Treatment typically focuses on addressing the underlying cause and may include cognitive rehabilitation and behavioral interventions.
Disorders, such as Down's Syndrome, are caused by nondisjunction.
No, Klinefelter syndrome and Turner syndrome are the result of nondisjunction of sex chromosomes. Klinefelter syndrome is caused by an extra X chromosome (XXY), while Turner syndrome is due to a missing X chromosome (XO).
There is no servant syndrome, It is likely that you are thinking albeit with bad spelling of Savant Syndrome. and it is recessive
The three major chromosomal disorders are Down syndrome, Turner syndrome, and Klinefelter syndrome. Down syndrome is characterized by an extra copy of chromosome 21, Turner syndrome involves a missing or incomplete X chromosome in females, and Klinefelter syndrome is caused by an extra X chromosome in males.
Deletion Syndrome or Williams Syndrome
Syndactyly is a characteristic of Apert syndrome, Poland syndrome, Jarcho-Levin syndrome, oral-facial-digital syndrome, Pfeiffer syndrome, and Edwards syndrome
Stockholm syndrome.
Syndactyly is a characteristic of Apert syndrome, Poland syndrome, Jarcho-Levin syndrome, oral-facial-digital syndrome, Pfeiffer syndrome, and Edwards syndrome.
XXXY Syndrome and Barr-Shaver-Carr Syndrome are the same.
Cushing's Syndrome
Disorders, such as Down's Syndrome, are caused by nondisjunction.
what is kinefelter syndrome?
yes there is.
Angelman syndrome is a genetic disorder, as is Down syndrome. But they are not the same. Angelman Syndrome involves a deletion of Chromosome 15, whereas people with Down syndrome have an extra copy of Chromosome 21.
also known as Martin-Bell syndrome, Marker X syndrome, and FRAXA syndrome
no
Alport Syndrome