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Hereditary and genetic
Reasoning that eminence is caused by genetic traits, he did a study of their heritability, publishing it in 1869 as Hereditary Genius.
The genetic basis of HD was discovered in 1993 by an international collaborative effort spearheaded by the Hereditary Disease Foundation.
Samoyeds can be affected by a genetic disease known as " Samoyed Hereditary Glomerulopathy ", a renal disease.
As yet there is no genetic screening test available for Samoyed Hereditary Glomerulopathy.
* Hereditary spherocytosis, a genetic disorder marked by hemolytic anemia
Due to the heavy influx of American Quarter Horse breeding, some Paints may also carry genetic disorders such as Hyperkalemic Periodic Paralysis ( HYPP ), Hereditary Equine Regional Dermal Asthenia ( HERDA ), Equine polysaccharide storage myopathy ( called PSSM-polysaccharide storage myopathy-in Paints, Quarter Horses and Appaloosas ), Malignant hyperthermia ( MH ) and Glycogen Branching Enzyme Deficiency ( GBED ).
Examples of genetic tendencies include Protein C deficiency, Protein S deficiency, the Factor V Leiden mutation, Hereditary anti-thrombin deficiency and Prothrombin Mutation G20210A.
Hereditary hemorrhagic telangiectasia ( HHT ), also known as Osler-Weber-Rendu disease and Osler-Weber-Rendu syndrome, is a genetic disorder that leads to abnormal blood vessel formation in the skin, mucous membranes, and often in organs such as the lungs, liver and brain.
Hereditary angioedema ( HAE ) exists in three forms, all of which are caused by a genetic mutation that is inherited in an autosomal dominant form.
Lynch syndrome ( HNPCC or Hereditary nonpolyposis colorectal cancer ) is an autosomal dominant genetic condition which has a high risk of colon cancer as well as other cancers including endometrium, ovary, stomach, small intestine, hepatobiliary tract, upper urinary tract, brain, and skin.
* inherited or genetic diseases ( Familial Dysautonomia, Hereditary Sensory Autonomic Neuropathy )
** Sub-specialties: Hereditary and genetic eye diseases
Hereditary inclusion body myopathies ( HIBM ) are a heterogeneous group of genetic disorders which have different symptoms.

Hereditary and disorders
Hereditary disorders causing ataxia include autosomal dominant ones such as spinocerebellar ataxia, episodic ataxia, and dentatorubropallidoluysian atrophy, as well as autosomal recessive disorders such as Friedreich's ataxia ( sensory and cerebellar, with the former predominating ) and Niemann Pick disease, ataxia-telangiectasia ( sensory and cerebellar, with the latter predominating ), and abetalipoproteinaemia.
:* The Hereditary spherocytosis ( HS ) syndromes are a group of inherited disorders characterized by the presence of spherical-shaped erythrocytes on the peripheral blood smear.
* Hereditary spastic paraplegia-a group of inherited disorders that are characterized by progressive weakness and stiffness of the legs
* Hereditary Spastic Paraplegia-a group of clinically and genetically diverse disorders that share a primary feature, which is the causation of progressive and generally severe lower extremity weakness and spasticity.
Hereditary disorders of all PPARs have been described, generally leading to a loss in function and concomitant lipodystrophy, insulin resistance, and / or acanthosis nigricans.
Hereditary inclusion body myopathies comprise both autosomal recessive and autosomal dominant muscle disorders that have a variable expression ( phenotype ) in individual patients, but all share similar structural features in the muscles.
Hereditary inclusion body myopathy ( IBM ) constitutes a unique group of neuromuscular disorders characterized by adult-onset slowly progressive distal and proximal weakness, and a typical muscle pathology including rimmed vacuoles and filamentous inclusions.

Hereditary and such
Can occur due to autosomal dominant diseases, such as Hereditary Hemorrhagic Telangiectasia.
The traditional official title, used until 1980, for other dynastic male heirs was Hereditary Prince of Sweden (), although the word prince () was used in constitutional legal texts such as the Instrument of Government of 1809 and also colloquially and informally.
Included are traditional stories about creation and other phenomena told by Aboriginal people such as Mi ' kmaq Hereditary Chief Stephen Augustine who recounts the beginning of the world in the Creation Stories Theatre film.
The Commons will occasionally bargain and negotiate with the Lords such as when the Labour Government of 1999 tried to expel all Hereditary Peers from the Lords, and the Lords threatened to wreck the Government's entire legislative agenda and to block every bill which was sent to the chamber.
At such time, he would receive the traditional titles of the heir-apparent to Monaco's throne, becoming HSH Hereditary Prince Andrea of Monaco, Marquis of Baux.
Several territories of the Empire were not represented, while some officials ( such as the Hereditary Usher ) were non-voting members ; neither qualified as Imperial States.
Hereditary aniridia is usually transmitted in an autosomal dominant manner ( each offspring has a 50 % chance of being affected ), although rare autosomal recessive forms ( such as Gillespie syndrome ) have also been reported.
The earliest such research, Hereditary Genius by Francis Galton ( 1869 ), argued that people vary hugely in “ natural ability ” which is inherited biologically.
The ruling or noble class of the Brigade ( referred to as " brazazz " or " brass ass ") bear titles that refer to the Brigade's former military organization based on officer ranks, such as " Hereditary Captain " or " Hereditary Colonel.
Christian ( 1818 – 1906 ), who in the 1840's became Hereditary Prince of Denmark ( though his brothers did not become such ) and in 1863 became King Christian IX of Denmark.
The titles of heirs apparent to a monarchy are treated as substantive titles, such as the Dutch Prince of Orange, Belgian Duke of Brabant, Spanish Prince of Asturias, British Prince of Wales, Danish Crown Prince, Luxemburgish Hereditary Grand Duke, and the Monégasque and Liechtensteiner Hereditary Princes.

Hereditary and type
* Dejerine – Sottas disease type of Hereditary motor and sensory neuropathy.
Hereditary angioedema type III has separate pathogenesis, being caused by mutations in F12 gene coding for a serine protease called Factor XII.
* Focal palmoplantar keratoderma with oral mucosal hyperkeratosis ( also known as " Hereditary painful callosity syndrome ," " Keratosis follicularis ," and " Keratosis palmoplantaris nummularis ") is an autosomal dominant keratoderma that represents a clinical overlap syndrome with pachyonychia congenita type I but without the classic nail involvement

Hereditary and 1
Other linked genes include the Hereditary Prostate cancer gene 1 ( HPC1 ), the androgen receptor, and the vitamin D receptor.
On 1 July 1844, the Hereditary Grand Duke Carl Alexander held a literary soiree at Ettersburg in honor of Andersen.
Of these 92, 1 is the Earl Marshal, a hereditary office always held by the Duke of Norfolk, 1 is the Lord Great Chamberlain, a hereditary office held in gross, currently by the Marquess of Cholmondeley, and the other 90 are elected by other Hereditary Peers.
She was christened Victoria Patricia Helena Elizabeth at Bagshot Park on 1 May 1886 and her godparents were: Queen Victoria ( her paternal grandmother ); the Duke of Saxe-Coburg and Gotha ( her paternal granduncle, who was represented by her paternal uncle Prince Christian of Schleswig-Holstein ); the Hereditary Grand Duchess of Oldenburg ( her maternal aunt ); Prince Wilhelm of Prussia ( her cousin, for whom the German Ambassador, Count Hatzfeldt, stood proxy ); Princess Christian of Schleswig-Holstein ( her paternal aunt ); and Prince Albert of Prussia ( her cousin, for whom her maternal uncle the Hereditary Grand Duke of Oldenburg stood proxy ).
Hereditary haemochromatosis is an autosomal recessive disorder with estimated prevalence in the population of 1 in 500 among patients with European ancestry, with lower incidence in other ethnic groups.
* Ferdinand Philippe, Hereditary Prince of Lorraine, suo jure Duke of Bar ( 29 December 1639 – 1 April 1659 )
Pes cavus is sometimes — but not always — connected through Hereditary Motor and Sensory Neuropathy Type 1 ( Charcot-Marie-Tooth disease ) and Friedreich's Ataxia ; many other cases of pes cavus are natural.
* 9 January 1938 – 1 April 1947: Her Royal Highness The Hereditary Princess of Greece, Princess of Denmark, Duchess of Sparta
# Karoline Luise ( b. Weimar, 18 July 1786-d. Ludwigslust, 20 January 1816 ), married on 1 July 1810 to Frederick Ludwig, Hereditary Grand Duke of Mecklenburg-Schwerin.
She was also Joint ( 1 / 4 ) Hereditary Lord Great Chamberlain from 1870 to her death.
On 1 November 1802, in Karlsruhe, Frederick William married Princess Marie Elisabeth of Baden ( 7 September 1782 Karlsruhe – 20 April 1808 Bruchsal ), daughter of Charles Louis, Hereditary Prince of Baden.

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