Ataxia crypta

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Ataxia crypta
Ataxia crypta SERC 06-06-16 (27276491020).jpg
Scientific classification Red Pencil Icon.png
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Coleoptera
Family: Cerambycidae
Subfamily: Lamiinae
Genus: Ataxia
Species:
A. crypta
Binomial name
Ataxia crypta
(Say, 1831)
Synonyms
  • Amniscus? cryptus(Say, 1832)
  • Ataxia sordidaHaldeman, 1847
  • Lamia cryptaSay, 1832
  • Leptostylus cryptus(Say, 1832)
  • Saperda annulataFabricius, 1801 nec 1792
  • Stenosoma sordidum(Haldeman, 1847)
  • Stenosoma crypta(Say, 1832) (misspelling)
  • Stenosoma sordida(Haldeman, 1847) (misspelling)
  • Ataxia lineata(Fabricius, 1792)

Ataxia crypta is a species of beetle in the family Cerambycidae. It was described by Thomas Say in 1831, originally under the genus Lamia . It is known from the United States and Mexico. [1]

Related Research Articles

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. Ataxia is a clinical manifestation indicating dysfunction of the parts of the nervous system that coordinate movement, such as the cerebellum. Ataxia can be limited to one side of the body, which is referred to as hemiataxia. Several possible causes exist for these patterns of neurological dysfunction. Dystaxia is a mild degree of ataxia. Friedreich's ataxia has gait abnormality as the most commonly presented symptom. The word is from Greek α- [a negative prefix] + -τάξις [order] = "lack of order".

Crypt Stone chamber or vault beneath the floor of a burial vault

A crypt is a stone chamber beneath the floor of a church or other building. It typically contains coffins, sarcophagi, or religious relics.

Crypta Neapolitana

The Crypta Neapolitana, is an ancient Roman road tunnel near Naples, Italy. It was built in 37 BC, and is over 700 metres long.

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.

Friedreichs ataxia Rare autosomal-recessive human disease

Friedreich's ataxia is an autosomal-recessive genetic disease that causes difficulty walking, a loss of sensation 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, people lose their sight and hearing. Other complications include scoliosis and diabetes mellitus.

Spinocerebellar ataxia Medical condition

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.

Fossa, Abruzzo Comune in Abruzzo, Italy

Fossa is a comune and town in the province of L'Aquila in the Abruzzo region of southern Italy. Bernardino of Fossa was born in the town.

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.

Theatre of Balbus

Theatre of Balbus was an ancient Roman structure in the Campus Martius of Rome. It was built in 13 BC by proconsul Lucius Cornelius Balbus (minor), likely from the spoils of a military campaign by order of Augustus.

<i>Ataxia</i> (beetle) Genus of beetles

Ataxia, described by Haldeman in 1847, is an American genus of longhorn beetles of the subfamily Lamiinae, tribe Pteropliini.

The cryptic flycatcher is a species of bird in the family Muscicapidae. It is endemic to the Philippines.

Ca<sub>v</sub>2.1

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.

KCNC3

Potassium voltage-gated channel, Shaw-related subfamily, member 3 also known as KCNC3 or Kv3.3 is a protein that in humans is encoded by the KCNC3.

<i>Ataxia</i> (album) 2008 studio album by Circus Devils

Ataxia is the sixth studio album released by 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.

Acetergamine Chemical compound

Acetergamine is an organic chemical compound; specifically it is a derivative of ergoline, making it a member of the ergotamine family of compounds. Acetergamine currently has no mainstream uses, however its potential as an alpha-1 blocker and vasodilator has led to it being covered in several patents concerning therapies for erectile dysfunction. It has also been investigated as a treatment for cerebellar ataxia.

Truncal ataxia Wide-based "drunken sailor" gait symptom

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.

Pyrola crypta, commonly known as cryptic wintergreen, is a perennial herb in the heath family.

Scythris crypta is a species of moth belonging to the family Scythrididae.

References

  1. BioLib.cz - Ataxia crypta. Retrieved on 8 September 2014.