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== Diagnosis ==
== Diagnosis ==
Unusually short stature for a child's age is usually what brings the child to medical attention. Skeletal [[dysplasia]] ("dwarfism") is usually suspected because of obvious physical features (e.g., unusual configuration of face or shape of skull), because of an obviously affected parent, or because body measurements (arm span, upper to lower segment ratio) indicate disproportion. Bone x-rays are often the key to diagnosis of a specific skeletal dysplasia, but they are not the key diagnosis. Most children with suspected skeletal dysplasias will be referred to a genetics clinic for diagnostic confirmation and [[genetic counseling]]. (See [[#External links|External links]], below, for a list of American referral centers with special expertise in skeletal dysplasias.) In the last decade, genetic tests for some of the specific disorders have become available.
Unusually short stature for a child's age is usually what brings the child to medical attention. Skeletal [[dysplasia]] ("dwarfism") is usually suspected because of obvious physical features (e.g., unusual configuration of face or shape of skull), because of an obviously affected parent, or because body measurements (arm span, upper to lower segment ratio) indicate disproportion. Bone x-rays are often the key to diagnosis of a specific skeletal dysplasia, but they are not the key diagnosis. Most children with suspected skeletal dysplasias will be referred to a genetics clinic for diagnostic confirmation and [[genetic counseling]]. (See [[#External links|External links]], below, for a list of American referral centers with special expertise in skeletal dysplasias.) In the last decade, genetic tests for some of the specific disorders have become available.
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During the initial medical evaluation for shortness, the absence of disproportion and the other clues above usually indicates other causes than bone dysplasias. Extreme shortness with completely normal proportions sometimes indicates [[growth hormone deficiency]] (''pituitary dwarfism).''
During the initial medical evaluation for shortness, the absence of disproportion and the other clues above usually indicates other causes than bone dysplasias. Extreme shortness with completely normal proportions sometimes indicates [[growth hormone deficiency]] (''pituitary dwarfism).''



Revision as of 01:52, 22 February 2008

Dwarfism
SpecialtyMedical genetics Edit this on Wikidata

Dwarfism refers to a condition of extreme small size of an animal, or plant. Any type of marked human smallness could be termed dwarfism in older popular and medical usage. The term as related to human beings (the major subject of this article) is often used to refer specifically to those forms of extreme shortness characterized by disproportion of body parts, typically due to an inheritable disorder in bone or cartilage development.

Forms of extreme shortness characterized by proportional body parts usually have a hormonal or nutritional cause. An example is growth hormone deficiency, once known as "pituitary dwarfism".

The Little People of America (LPA) defines dwarfism as a medical or genetic condition that usually results in an adult height of 4'10" (147 cm) or shorter.[1]

Types of dwarfism

  • rhizomelic = root, e.g. bones of upper arm or thigh
  • mesomelic = middle, e.g. bones of forearm or lower leg
  • acromelic = end, e.g. bones of hands and feet.

When the cause of dwarfism is understood, it may be classified according to one of hundreds of names, which are usually permutations of the following roots:

  • chondro = of cartilage
  • osteo = of bone
  • spondylo = of the vertebrae
  • plasia = form
  • trophy = growth

Examples include achondroplasia, osseous dysplasia, chondrodystrophy, and osteochondrodystrophy.[2]

The most recognizable and most common form of dwarfism is achondroplasia, which produces rhizomelic short limbs, increased spinal curvature, and distortion of skull growth. It accounts for 70% of dwarfism cases. Other relatively common types include spondyloepiphyseal dysplasia congenita (SED), diastrophic dysplasia, pseudoachondroplasia, hypochondroplasia, and osteogenesis imperfecta (OI). Severe shortness with skeletal distortion also occurs in several of the mucopolysaccharidoses and other storage diseases.

The average adult height of male and females with dwarfism is 132cm and 123cm respectively. The average weight of an adult may range from 100 to 150 pounds (45-68 kg).

Diagnosis

Unusually short stature for a child's age is usually what brings the child to medical attention. Skeletal dysplasia ("dwarfism") is usually suspected because of obvious physical features (e.g., unusual configuration of face or shape of skull), because of an obviously affected parent, or because body measurements (arm span, upper to lower segment ratio) indicate disproportion. Bone x-rays are often the key to diagnosis of a specific skeletal dysplasia, but they are not the key diagnosis. Most children with suspected skeletal dysplasias will be referred to a genetics clinic for diagnostic confirmation and genetic counseling. (See External links, below, for a list of American referral centers with special expertise in skeletal dysplasias.) In the last decade, genetic tests for some of the specific disorders have become available. i lick my mothers pooh During the initial medical evaluation for shortness, the absence of disproportion and the other clues above usually indicates other causes than bone dysplasias. Extreme shortness with completely normal proportions sometimes indicates growth hormone deficiency (pituitary dwarfism).

Short stature alone, in the absence of any other abnormalities, may simply be genetic, particularly if a person is born into a family of people who are relatively short.

Problems associated with dwarfism

The principal adverse effects of dwarfism can be divided into the physical and the social.

Physical effects of malformed bones vary according to the specific disease. Many involve pain resulting from joint damage from abnormal bone alignment, or from nerve compression (e.g, spinal stenosis).[1]. Early degenerative joint disease, exaggerated lordosis or scoliosis, and constriction of spinal cord or nerve roots can cause pain and disability. Reduced thoracic size can restrict lung growth and reduce pulmonary function. Some forms of dwarfism are associated with disordered function of other organs, such as the brain or liver, sometimes severely enough to be more disabling than the abnormal bone growth.

A dwarf is associated with the height 4'10" and under.

The psychosocial disadvantages may be more distressing than the physical symptoms, especially in childhood and adolescence, but people with dwarfism vary greatly in the degree to which social participation and emotional health are affected.

  • Social prejudice against extreme shortness may reduce social and marital opportunities.
  • Numerous studies have demonstrated reduced employment opportunities. Severe shortness is associated with lower income.[citation needed]
  • Self-esteem may be reduced and family relationships affected
  • Extreme shortness (in the low 2–3 foot [60–90 cm] range) can interfere with ordinary activities of daily living, like driving or even using countertops built for taller people.

Treatment and support

As the genetic defects of most forms of dwarfism due to bone dysplasia cannot be corrected, therapeutic interventions are typically aimed at (1) preventing or reducing pain or physical disability, (2) increasing adult height, or (3) mitigating psychosocial stresses and enhancing social adaptation.

Pain and disability may be ameliorated by physical therapy, by braces or other orthotic devices, or by surgical procedures. The only simple interventions that increase perceived adult height are dress enhancements such as shoe lifts or hairstyle. Growth hormone is rarely used for shortness due to bone dysplasias, as the height benefit is typically small (less than 5 cm) and the cost high. The most effective means of increasing adult height by several inches is limb-lengthening surgery, though availability is limited and cost is high in terms of dollars, discomfort, and interruption of life. Most people with dwarfism do not avail themselves of this, and it remains controversial.[1] For other types of dwarfism, surgical treatment is not possible.

Dwarfism in non-Western cultures

In the Talmud, it is said that the second born son of the Egyptian Pharaoh of the Bible was a dwarf.[3]

File:Velazquez-dwarf-don-sebastian-de-morra.jpg
The Dwarf Don Sebastián de Morra, by Velázquez. In his portraits of the dwarves of Spain's royal court, the artist preferred a serious tone.
"Queen Henrietta Maria and the dwarf Sir Jeffrey Hudson",by Anthonis van Dyck, 1633

When depicted in art, literature, or movies, dwarves are rarely depicted as "regular people who are very short" but often as a species apart. Novelists, artists, and moviemakers attach special moral or aesthetic significance to the "apartness" or the misshapenness.

Artistic representations of dwarfism can be found on Greek vases and other ancient artefacts, including ancient Egyptian art. Documentation of dwarves can also be found on European paintings and many pictures. Many European paintings (especially Spanish) of the 16th19th centuries depict dwarves by themselves or with others.

In Jonathan Swift's "Gulliver's Travels", the protagonist encounters in the court of the Giants' Kingdom the strong enmity of the local "dwarf", who is "only" twenty feet high (where normal giants measure forty feet) and resents being displaced by "a smaller dwarf".

Several novels have treated dwarfism as a major theme, although not necessarily realistically:

Leslie Fiedler's Freaks: Myths and Images of the Secret Self (1979) explored the value of differentness of "freaks" to "normal" people, lamenting medical treatment for reducing the number of picturesquely different people around.

Several 20th and 21st century movies & TV shows have addressed the topic or made much use of dwarves:

The actor and stunt man Verne Troyer has become famous playing the character "Mini-Me" in two Austin Powers movies, as has fellow stuntman and Jackass cast-member, Jason "Wee-Man" Acuña .

The 1960s television series The Wild Wild West featured a dwarf, Michael Dunn, as the recurring character Dr. Miguelito Loveless, the brilliant but insane arch-enemy of Secret Service agents James West and Artemus Gordon.

In the mid-1970's, Sid and Marty Krofft built an indoor theme park in Atlanta, Georgia called The World of Sid and Marty Krofft. This had a live stage production that was at that time the largest gathering of "little people" since the filming of The Wizard of Oz in 1937-38 as well as being the largest indoor theme park built to that time. The facility that was built to house this theme park is today the studios of CNN, the Cable News Network, and CNN Headline News.

In the 1990s, the immensely popular series Seinfeld featured a dwarf character, Mickey Abbott, in seven episodes; Mickey was played by actor Danny Woodburn. He got into several physical altercations with six-foot-plus Kramer. In one episode, he was ostracized by his dwarf peers for using lifts in his shoes to make him look taller.

In the movie, The Mighty, one of the main characters, Kevin, nicknamed Freak, has a rare form of dwarfism called Morquio syndrome, which kills him at the end of the movie because of the symptoms.

Arguably the most famous dwarf actor is Warwick Davis, having found success in several notable fantasy franchises, including Star Wars, Harry Potter, Willow, Leprechaun, Gulliver's Travels, and The Chronicles of Narnia (both the 1989 television serial and again in the upcoming 2008 film version of Prince Caspian).

From 1999 until 2003, the popular television series The Man Show featured dwarves in many of their segments. They once claimed to be "the world's largest employer of midgets".

In Mind of Mencia, one of the main characters is a dwarf named Brad Williams. Brad is a comedian who tours with Carlos Mencia as his opening act.

In Monster Garage, Chris "Body Drop" Artiaga made his début as a contestant in episode 'Ramp Rage', but later became parts runner for the series. In addition, there are 2 episodes featuring all-dwarf build teams.

In George R.R. Martin's A Song of Ice and Fire series, one of the main characters, Tyrion Lannister, is a dwarf. Though a brilliant and well-read man (some would say genius), he struggles with acceptance by "normal" people, who pejoratively refer to him as "the Imp," or "half-man". This is especially true of his father, Lord Tywin Lannister, who holds Tyrion in contempt, especially when compared to Tyrion's handsome, talented older brother Jaime, and Jaime's equally beautiful and talented twin sister, Cersei. Tyrion often wonders if any woman could ever truly love him in spite of his condition.

Johnny Roventini was a dwarf bellboy in a New York City hotel when he was paid $1 to "Call for Phillip Morris", unknowingly beginning his 40-year career as an advertising icon in radio, television, and print media.

See also

References

  1. ^ a b c "Dwarfism Resources: Frequently Asked Questions". Little People of America. 2006-7-9. Archived from the original on 2007-07-12. Retrieved 2006-11-14. {{cite web}}: Check date values in: |date= (help)
  2. ^ "Dwarfism and Dysplasias - Wheeless' Textbook of Orthopaedics". Retrieved 2007-12-07.
  3. ^ The Talmud - CHAPTER VI. DEATH OF JACOB AND HIS SONS--MOSES--THE DELIVERANCE FROM EGYPT. URL accessed April 23, 2007