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  2. Choroideremia - Wikipedia

    en.wikipedia.org/wiki/Choroideremia

    Choroideremia (/ k ɒ ˌ r ɔɪ d ɪ ˈ r iː m i ə /; CHM) is a rare, X-linked recessive form of hereditary retinal degeneration that affects roughly 1 in 50,000 males. The disease causes a gradual loss of vision, starting with childhood night blindness , followed by peripheral vision loss and progressing to loss of central vision later in life.

  3. List of neuroscience databases - Wikipedia

    en.wikipedia.org/wiki/List_of_neuroscience_databases

    A number of online neuroscience databases are available which provide information regarding gene expression, neurons, macroscopic brain structure, and neurological or psychiatric disorders. Some databases contain descriptive and numerical data, some to brain function, others offer access to 'raw' imaging data, such as postmortem brain sections ...

  4. Choroid plexus - Wikipedia

    en.wikipedia.org/wiki/Choroid_plexus

    The choroid plexus regulates the production and composition of cerebrospinal fluid (CSF), that provides the protective buoyancy for the brain. [2] [10] CSF acts as a medium for the glymphatic filtration system that facilitates the removal of metabolic waste from the brain, and the exchange of biomolecules and xenobiotics into and out of the brain.

  5. Ayazi syndrome - Wikipedia

    en.wikipedia.org/wiki/Ayazi_syndrome

    Choroideremia-deafness-obesity syndrome This condition is inherited in an X-linked recessive manner. Ayazi syndrome (or Chromosome 21 Xq21 deletion syndrome ) [ 1 ] is a syndrome characterized by choroideremia , congenital deafness and obesity .

  6. Category:Disorders of choroid and retina - Wikipedia

    en.wikipedia.org/wiki/Category:Disorders_of...

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  7. Leukoencephalopathy - Wikipedia

    en.wikipedia.org/wiki/Leukoencephalopathy

    Leukoencephalopathy (leukodystrophy-like diseases) is a term that describes all of the brain white matter diseases, whether their molecular cause is known or unknown. [1] It can refer specifically to any of these diseases: Progressive multifocal leukoencephalopathy; Toxic leukoencephalopathy

  8. Usher syndrome - Wikipedia

    en.wikipedia.org/wiki/Usher_syndrome

    Usher syndrome, also known as Hallgren syndrome, Usher–Hallgren syndrome, retinitis pigmentosa–dysacusis syndrome or dystrophia retinae dysacusis syndrome, [1] is a rare genetic disorder caused by a mutation in any one of at least 11 genes resulting in a combination of hearing loss and visual impairment.

  9. Intraocular hemorrhage - Wikipedia

    en.wikipedia.org/wiki/Intraocular_hemorrhage

    Intraocular hemorrhage is classified based on the location of the bleeding: Hyphema (in the anterior chamber); Suprachoroidal hemorrhage (SCH) is a rare complication of intraocular surgery in which blood from the ciliary arteries enters the space between the choroid and the sclera.