Hereditary spastic paraplegias are classified based on the symptoms ; on their mode of inheritance ; on the patient ’ s age at onset ; and, ultimately, on the gene associated with the condition.

# REDIRECT Hereditary spastic paraplegia

# REDIRECT Hereditary spastic paraplegia

* Type V is appears to resemble Hereditary Spastic Paraplegia ; however, more research is needed to conclude the relationship between Type V MJD and hereditary spastic paraplegia.

:* 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 ( HSP ), also called Familial Spastic Paraplegias or Strumpell-Lorrain disease, is a group of inherited diseases whose main feature is progressive stiffness and contraction ( spasticity ) in the lower limbs, as a result of damage to dysfunction of the nerves.

* 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.

On 24 June 1928, a group of 12 Russian Hereditary Commanders met in Paris to re-establish the activities of the Russian Grand Priory.

Hereditary inclusion body myopathies ( HIBM ) are a heterogeneous group of genetic disorders which have different symptoms.

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.

Charcot-Marie-Tooth disease ( CMT ), also known as Hereditary Motor and Sensory Neuropathy ( HMSN ), Hereditary Sensorimotor Neuropathy ( HMSN ), or Peroneal Muscular Atrophy, is a heterogeneous inherited disorder of nerves ( neuropathy ) that is characterized by loss of muscle tissue and touch sensation, predominantly in the feet and legs but also in the hands and arms in the advanced stages of disease.

Hereditary polioencephalomyelopathy of the Australian Cattle Dog is a very rare condition caused by an inherited biochemical defect.

Hereditary ( inherited ) hemolytic anemia can be due to membrane defects:

Hereditary ( inherited ) hemolytic anemia can be due to defects in hemoglobin:

Hereditary ( inherited ) hemolytic anemia can be due to enzyme defects:

The earliest such research, Hereditary Genius by Francis Galton ( 1869 ), argued that people vary hugely in “ natural ability ” which is inherited biologically.

Hereditary angioedema ( HAE ) exists in three forms, all of which are caused by a genetic mutation that is inherited in an autosomal dominant form.

* Hereditary nobility — routinely inherited by heirs

* inherited or genetic diseases ( Familial Dysautonomia, Hereditary Sensory Autonomic Neuropathy )

* Diffuse nonepidermolytic palmoplantar keratoderma ( also known as " Diffuse orthohyperkeratotic keratoderma ," " Hereditary palmoplantar keratoderma ," " Keratosis extremitatum progrediens ," " Keratosis palmoplantaris diffusa circumscripta ," " Tylosis ," and " Unna-Thost disease ") is inherited as an autosomal dominant condition and is present from infancy, characterized by a well-demarcated, symmetric, often " waxy " keratoderma involving the whole of the palms and soles

Some members of the Lee Family Council chose his eldest son, Yi Won as the next Head of Korean Imperial Household and they also made his title the Hereditary Prince Imperial ( Hwangsason ) in the meaning of inherited a title of Prince Gu ( born 29 December 1931 – 16 July 2005 ).

On 16 July 2005, following the death of Prince Gu, some members of the Lee Family Council chose him as the next Head of Korean Imperial Household and they also made his title the Hereditary Prince Imperial ( Hwangsason ) in the meaning of inherited a title of Prince Gu.

* the Hereditary Seneschal ( vested in a living O ' Donnell, who was already ennobled as a Knight of Malta, and who inherited the Seneschalship from his father ), which survives under the auspices of the Hereditary Great Seneschal or Lord High Steward of Ireland, the Premier Earl of Ireland ( Chetwynd-Talbot ), who is the Earl of Shrewsbury, Waterford and Talbot, and is senior direct descendant of the 2nd Earl of Tyrconnell ( extinct ), and senior kin of the Duke of Tyrconnel Richard Talbot ( extinct ),

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.

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 ).

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 genetic disorders such as neurofibromatoses ( type 1 and type 2 ) and tuberous sclerosis complex are known to predispose to their development.

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.

The male-line descendants of Grand Duchess Charlotte who are the children of a reigning Grand Duke or The Hereditary Grand Duke hold the titles Prince ( ss ) of Luxembourg and Prince ( ss ) of Nassau with the style of His / Her Royal Highness.

Male line descendants of Grand Duchess Charlotte who are not the children of a Grand Duke or Hereditary Grand Duke are Prince ( ss ) of Nassau with the style of His / Her Royal Highness ( coming from their status as male-line descendants of Duke Robert of Parma ).

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.

Hereditary abnormalities of fibrinogen ( the gene is carried on chromosome 4 ) are of both quantitative and qualitative in nature and include afibrinogenaemia, hypofibrinogenaemia, dysfibrinogenaemia, and hypodysfibrinogenaemia.

Staffordshire Bull Terriers are known to suffer from Hereditary Cataracts ( HC ) and L-2-hydroxyglutaric aciduria ( L2HGA )— a metabolic disorder resulting in behavioural changes and dementia-like symptoms — both of which are detectable via DNA tests.

The various individuals who hold fractions of the Lord Great Chamberlainship are technically each Joint Hereditary Lord Great Chamberlain, and the right to exercise the office for a given reign rotates proportionately to the fraction of the office held.

Horemheb's specific titles are outlined from his Saqqara tomb which was built while he was still only an official: " Hereditary Prince, Fan-bearer on the Right Side of the King, and Chief Commander of the Army "; the " attendant of the King in his footsteps in the foreign countries of the south and the north "; the " King's Messenger in front of his army to the foreign countries to the south and the north "; and the " Sole Companion, he who is by the feet of his lord on the battlefield on that day of killing Asiatics.

When Tutankhamun died while still a teenager, Horemheb had already been officially designated as the rpat or iry-pat ( basically the " Hereditary or Crown Prince ") and idnw (" Deputy of the King " in the entire land ) by the child pharaoh ; these titles are found inscribed in Horemheb's then private Memphite tomb at Saqqara which dates to the reign of Tutankhamun since the child king's ...

The children are, respectively, second, fourth and third in the line of succession to the Monegasque throne, after their mother, HRH the Princess of Hanover, Hereditary Princess of Monaco.

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 Marquesses are also Hereditary Constables of Hillsborough Fort.

Hereditary spherocytosis is a genetically-transmitted ( autosomal dominant ) form of spherocytosis, an auto-hemolytic anemia characterized by the production of red blood cells that are sphere-shaped rather than bi-concave disk shaped ( Donut-Shaped ), and therefore more prone to hemolysis.

Hereditary spherocytosis is an autosomal dominant or recessive trait, most commonly ( though not exclusively ) found in Northern European and Japanese families, although an estimated 25 % of cases are due to spontaneous mutations.

Hereditary supporters are normally limited to hereditary peers, certain members of the Royal Family, chiefs of Scottish Clans, Scottish feudal barons whose baronies predate 1587.

Among his 29 titles are: Master of the Royal Household of Scotland and Hereditary Keeper of the Great Seal of Scotland ( ranking 25th in the Scottish Order of Precedence ), Admiral of the Western Coasts and Isles, and the Chief of Clan Campbell.

The Hereditary Chiefs who are leading Tla-o-qui-aht through this process are:

There is currently a standing agreement that decisions regarding resource use are done through consensus of the six Hereditary Chiefs.

Currently, regionally focused appointments are made by the Hereditary Chiefs.