| Ataxia hubbardi | |
|---|---|
 | |
Scientific classification  | |
| Domain: | Eukaryota |
| Kingdom: | Animalia |
| Phylum: | Arthropoda |
| Class: | Insecta |
| Order: | Coleoptera |
| Infraorder: | Cucujiformia |
| Family: | Cerambycidae |
| Subfamily: | Lamiinae |
| Tribe: | Pteropliini |
| Genus: | Ataxia |
| Species: | A. hubbardi |
| Binomial name | |
| Ataxia hubbardi Fisher, 1924 | |
| Synonyms | |
| |
Ataxia hubbardi is a species of beetle in the family Cerambycidae. It was described by Warren Samuel Fisher in 1924. It is known from the United States and Mexico. [1]
Ataxia is a neurological sign consisting of lack of voluntary coordination of muscle movements that can include gait abnormality, speech changes, and abnormalities in eye movements, that indicates dysfunction of parts of the nervous system that coordinate movement, such as the cerebellum.
Ataxia–telangiectasia, also referred to as ataxia–telangiectasia syndrome or Louis–Bar syndrome, is a rare, neurodegenerative, autosomal recessive disease causing severe disability. Ataxia refers to poor coordination and telangiectasia to small dilated blood vessels, both of which are hallmarks of the disease. A–T affects many parts of the body:
Friedreich's ataxia is an autosomal-recessive genetic disease that causes difficulty walking, a loss of coordination in the arms and legs, and impaired speech that worsens over time. Symptoms generally start between 5 and 20 years of age. Many develop hypertrophic cardiomyopathy and require a mobility aid such as a cane, walker, or wheelchair in their teens. As the disease progresses, some affected people lose their sight and hearing. Other complications may include scoliosis and diabetes mellitus.
Spinocerebellar ataxia (SCA) is a progressive, degenerative, genetic disease with multiple types, each of which could be considered a neurological condition in its own right. An estimated 150,000 people in the United States have a diagnosis of spinocerebellar ataxia at any given time. SCA is hereditary, progressive, degenerative, and often fatal. There is no known effective treatment or cure. SCA can affect anyone of any age. The disease is caused by either a recessive or dominant gene. In many cases people are not aware that they carry a relevant gene until they have children who begin to show signs of having the disorder.
Sensory ataxia is both a symptom and a sign in neurology. It is a form of ataxia caused not by cerebellar dysfunction but by loss of sensory input into the control of movement.
Cerebellar ataxia is a form of ataxia originating in the cerebellum. Non-progressive congenital ataxia (NPCA) is a classical presentation of cerebral ataxias.
Episodic ataxia (EA) is an autosomal dominant disorder characterized by sporadic bouts of ataxia with or without myokymia. There are seven types recognized but the majority are due to two recognized entities. Ataxia can be provoked by psychological stress or startle, or heavy exertion, including exercise. Symptoms can first appear in infancy. There are at least six loci for EA, of which 4 are known genes. Some patients with EA also have migraine or progressive cerebellar degenerative disorders, symptomatic of either familial hemiplegic migraine or spinocerebellar ataxia. Some patients respond to acetazolamide though others do not.
The Coqui francolin is a species of bird in the family Phasianidae.
Ataxia, described by Haldeman in 1847, is an American genus of longhorn beetles of the subfamily Lamiinae, tribe Pteropliini.
Cav2.1, also called the P/Q voltage-dependent calcium channel, is a calcium channel found mainly in the brain. Specifically, it is found on the presynaptic terminals of neurons in the brain and cerebellum. Cav2.1 plays an important role in controlling the release of neurotransmitters between neurons. It is composed of multiple subunits, including alpha-1, beta, alpha-2/delta, and gamma subunits. The alpha-1 subunit is the pore-forming subunit, meaning that the calcium ions flow through it. Different kinds of calcium channels have different isoforms (versions) of the alpha-1 subunit. Cav2.1 has the alpha-1A subunit, which is encoded by the CACNA1A gene. Mutations in CACNA1A have been associated with various neurologic disorders, including familial hemiplegic migraine, episodic ataxia type 2, and spinocerebellar ataxia type 6.
Ataxia is the sixth studio album released by the American alternative/psychedelic rock band Circus Devils on October 31, 2008. All songs on Ataxia were written and performed by Robert Pollard, Todd Tobias, and Tim Tobias.
Evalljapyx hubbardi is a species of forcepstail in the family Japygidae. It is found in North America.
Discostrobilops hubbardi is a land snail of the Americas - colloquially known as the Flatten Pinecone. It was formerly known as Strobilops hubbardi, but that taxon is no longer in use. It is known to be found in Southern parts of the United States, including Georgia, Alabama, and Florida. It was confirmed in 2018 to be living in South Texas.
Colon hubbardi is a species of round fungus beetle in the family Leiodidae. It is found in North America.
Marginitermes hubbardi, commonly known as the light western drywood termite, is a species of termite in the family Kalotermitidae. It is found in Central America and desert regions of southwestern North America.
David A. Hubbard, Jr is an American speleobiologist and karst geologist, exploring and documenting speological sites and life forms around Virginia and Maryland. He has published on phenomenon of burial caves, in particular by the indigenous peoples of Virginia, as well as the use of caves by human beings over the past 10,500 years.
Usazoros hubbardi, commonly known as Hubbard's angel insect, is a species of insect in the order Zoraptera. It is native to the tropical and subtropical New World and has expanded its range into the eastern United States, where it lives in piles of sawdust, whereas in the hotter part of its range it lives under the bark of decomposing logs. It was named after the American entomologist Henry Guernsey Hubbard, who discovered the insect in the United States.
Truncal ataxia is a wide-based "drunken sailor" gait characterised by uncertain starts and stops, lateral deviations and unequal steps. It is an instability of the trunk and often seen during sitting. It is most visible when shifting position or walking heel-to-toe.
Pterotermes is a monotypic genus of termites in the family Kalotermitidae. Pterotermes occidentis is the single species in the genus. This termite lives in the extremely dry conditions found in the Sonoran Desert in southwestern United States, Baja California and Mexico. It feeds on dry wood and lives entirely within a single piece of timber.
Cirrhitops hubbardi, Hubbard's hawkfish or the white-spotted hawkfish is a species of marine ray-finned fish, a hawkfish belonging to the family Cirrhitidae. It is found in the Western Pacific Ocean.
