Eingeschränktes Wachstum
Dwarfism
Begutachtet von Dr Colin Tidy, MRCGPZuletzt aktualisiert von Dr Hayley Willacy, FRCGP Last updated 15 Sept 2024
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Dwarfism is a medical or genetic condition which causes people to have restricted growth so that they are shorter than average. Specifically, people with dwarfism grow no higher than 4 ft 10 ins (147 cm).
It can be due to literally hundreds of different causes, so the term actually includes many different medical conditions. The cause and type of dwarfism will therefore affect the outlook and problems that may be associated with it. The most common condition causing dwarfism is achondroplasia.
At a glance
Restricted growth, also called dwarfism, means a person is significantly shorter than others of the same age.
Dwarfism usually means an adult height of 147 cm (4 ft 10 ins) or less.
It is caused by a genetic or medical condition, with achondroplasia being the most common cause.
There are two types: proportionate, where all body parts are small, and disproportionate, where limbs are noticeably shorter.
Most people with dwarfism have few major medical problems and lead full lives.
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What is restricted growth (dwarfism)?
Restricted growth is a medical condition causing people to grow less than others, so that they are shorter than those of the same age. It is also called dwarfism, or referred to as 'short stature'.
Dwarfism describes a person with an adult height of 4 ft 10 ins (147 cm) or less. You may see people with dwarfism referred to as dwarfs, little people, or people with short stature. These are generally used as descriptions rather than labels.
Types of dwarfism
Zurück zum InhaltDwarfism is usually broadly grouped into two different types depending on the body proportions:
Proportionate: there is a lack of growth in all of the body. All parts of the body are shorter than usual but are in proportion to each other. Other body functions are likely to be affected in addition to the growth process.
Disproportionate: the main part of the body (the trunk) is a reasonably normal size but the arms and legs are shorter than average. There is usually a genetic cause. This is the type caused by the condition called achondroplasia, which is the most common cause of dwarfism. Usually people with disproportionate dwarfism do not have associated learning disabilities.
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What causes dwarfism?
Zurück zum InhaltDwarfism is due to a genetic or medical condition, and there are hundreds of causes.
In a genetic cause there is a change (mutation) in the genes that form the code in our body's cells upon which all our physical characteristics are based. This can be a mutation inherited from our parents.
Usually dwarfism has a genetic cause, but in some cases other medical conditions can cause a problem with growth. This may occur as a baby is developing in the womb or after birth in childhood.
Some of the more common causes of dwarfism are:
Achondroplasie. This is a genetic condition causing disproportionate short stature. Upper arms and legs are shorter than average. It usually comes with other typical features such as a prominent forehead and relatively large head, limited elbow movement, and a curved spine. Intelligence and lifespan are not generally affected.
Diastrophic dysplasia (DTD). A rare genetic condition where limbs are shortened. It tends to be associated with other problems such as a cleft palate, club feet, chest abnormalities and abnormally shaped ears.
Spondo-epiphyseal dysplasia (SED). This is a group of conditions where the trunk is affected more than the limbs, due to a problem in the connective tissues of the joints. There may be other abnormalities. This may not be obvious at birth and may be picked up as the child grows.
Pseudoachondroplasia. This is an inherited condition and is likely to run in families. It is not usually apparent at birth, unlike achondroplasia. Limbs are shortened but other typical features of achondroplasia are not present. There is hypermobility of joints and there are often joint abnormalities and problems.
Turner-Syndrom. This is a genetic condition affecting girls only. As well as short height, there are typical physical features, and ovaries do not work normally. See the separate leaflet called Turner syndrome for more information.
Prader-Willi-Syndrom. This is a rare genetic condition with many features including learning disability, obesity, muscle difficulties and behavioural problems. It may also cause short stature.
Noonan syndrome. A rare genetic condition causing many problems as well as short stature. These include heart defects, excessive bleeding, and delays in development.
Brittle bone disease (osteogenesis imperfecta). A rare genetic condition where bones are not properly formed and break very easily.
Medical conditions affecting growth. Many medical problems can have an effect on growth. Disorders which affect hormones (particularly growth hormone), major organs (for example, kidney diseases), bones or the body's general functioning (metabolism) can slow growth.
How common is dwarfism?
Zurück zum InhaltIt is estimated that dwarfism occurs somewhere between one in every 15,000 and one in every 40,000 children born.
Achondroplasia is the most common cause. It is the cause in 7 out of 10 people with the condition.
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What are the symptoms of dwarfism?
Zurück zum InhaltThere are no symptoms of dwarfism as such, other than being shorter than others. Short height may affect self-esteem, leading to psychological issues.
If the short stature is part of a genetic condition, there may be associated symptoms, difficulties or medical problems. These vary widely depending on which of the many causes is the reason for the restricted growth.
Symptoms of achondroplasia
Possible problems associated with achondroplasia (the most common cause of dwarfism) include:
Recurring Ohreninfektionen.
Crowding of teeth, needing dental treatment.
Bowed legs causing walking difficulties or joint problems.
Fluid around the brain (hydrocephalus).
Back pain and/or numbness in the legs, due to excessive curving of the spine, or narrowed spaces for the nerves to pass through.
How is dwarfism diagnosed?
Zurück zum InhaltThis will partly depend on the reason for dwarfism. Babies born with achondroplasia are often diagnosed at birth, simply from their typical appearance. The most common tests used for diagnosis include:
Some people with dwarfism are diagnosed later in childhood, when it is noticed that they are not growing as much as other children of their age.
In making a diagnosis, doctors will take into account the pattern of growth, family history, other problems or features, findings on examination, blood tests and sometimes X-rays. Often blood tests for genetic conditions will be needed.
Some genetic conditions are suspected from tests done while the baby is still in the womb, and can be checked by tests done even before birth.
What is the treatment for dwarfism?
Zurück zum InhaltDwarfism in itself is not a disease that needs a 'cure'. It is a condition which in some cases may be caused by a disease, so sometimes treatments may be needed.
For most people with dwarfism, treatment for growth itself is not possible or helpful. Most people will adapt their way of life to cope with their less than average height, but otherwise lead entirely normal lives.
Treatment that might be relevant includes:
Wachstumshormon
This is treatment with a hormone medicine which aims to replace the growth hormone normally produced by the body. This is only helpful in a few specific causes of dwarfism where the lack of growth is caused by a lack of growth hormone. It is not helpful for people with achondroplasia. It is a treatment recommended by and managed by a specialist doctor.
Operation
Rarely, an operation may be done to lengthen the bones of the legs. This is not commonly done as it involves breaking the leg bones and is a lengthy treatment with a number of risks.
Other operations for bones are sometimes needed to correct associated problems. For example, for people with bow legs, operations are sometimes needed to straighten the legs.
Operations on the back may be needed to give more space for the nerves to pass through and to relieve pain. Other operations are sometimes needed to correct other associated medical issues, such as to release the fluid around the brain in people with hydrocephalus.
Team management
For a person with an unusual syndrome resulting in a number of medical problems, often a team of health professionals is involved to help.
This might involve:
Speech therapists.
Dieticians.
Nurses.
Specialist doctors.
Support groups
In many countries there are websites for support groups with more information for people either with dwarfism or with the specific conditions causing it. Some of those in the UK are listed in the further reading section below.
You can feel rather 'on your own' if you or your child have a very rare condition, and you may find this information and support network very helpful.
Wie ist der Ausblick?
Zurück zum InhaltThe outlook (or prognosis) entirely depends on the underlying condition. Overall, most people with dwarfism have no major medical problems, and live full and healthy normal lives.
Dwarfism life expectancy
Life expectancy is normal in achondroplasia. However, some of the conditions which cause dwarfism can have associated medical issues which can significantly affect abilities and health.
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Entwicklungsdyspraxie (DCD), auch bekannt als Dyspraxie, ist eine häufige Erkrankung, die hauptsächlich die motorische Koordination betrifft – die Art und Weise, wie der Körper Bewegungsaufgaben organisiert und ausführt. Sie kann auch andere Aktivitäten beeinflussen, einschließlich der Sprache. Dyspraxie tritt bei Kindern und Erwachsenen auf. Dyspraxie bedeutet schlechte Koordination, aber der Begriff 'Dyspraxie' wird häufig verwendet, um die entwicklungsbedingte Dyspraxie bei Kindern zu beschreiben. Gesundheitsfachkräfte nennen dies heute Entwicklungskoordinationsstörung, um sie von ähnlichen Problemen (ebenfalls Dyspraxie genannt) zu unterscheiden, die durch andere medizinische Zustände verursacht werden – zum Beispiel Bewegungsprobleme nach Kopfverletzungen oder Schlaganfällen. In diesem Flyer verwenden wir jedoch den gebräuchlichen Begriff 'Dyspraxie', um auf die kindliche DCD Bezug zu nehmen. Zusätzlich wird Dyspraxie bei Kindern von Gesundheitsfachkräften manchmal als 'spezifische Entwicklungsstörung der motorischen Funktionen' (SDDMF) bezeichnet.
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Häufig gestellte Fragen
Is "dwarfism" considered an offensive term?
The article states that terms like "dwarfs," "little people," or "people with short stature" are generally used as descriptions rather than labels. This suggests these terms are acceptable, with an emphasis on respectful usage.
Can dwarfism be prevented, particularly if it's genetic?
The article explains that dwarfism is due to genetic or medical conditions, often involving a gene mutation. While it describes causes, it does not suggest that dwarfism can be prevented, especially when genetic in origin.
Are there any impacts on intelligence or lifespan for people with dwarfism?
The article mentions that for achondroplasia, intelligence and lifespan are not generally affected. However, it also clarifies that some conditions causing dwarfism can have associated medical issues that might significantly affect abilities and health. The outlook generally depends on the underlying condition.
If someone has dwarfism due to a medical condition rather than a genetic one, is the approach different?
The article notes that medical problems affecting growth can be a cause of dwarfism, such as disorders affecting hormones or major organs. While it details genetic causes more extensively, it indicates that a team of health professionals might be involved in management for someone with an unusual syndrome resulting in multiple medical problems, suggesting a comprehensive approach regardless of the origin.
What kind of everyday adjustments might be helpful for someone with restricted growth?
The article mentions that most people with dwarfism will adapt their way of life to cope with their height, leading entirely normal lives. While it doesn't list specific adjustments, it implies practical adaptations are common.
What support is available for individuals and families affected by dwarfism?
The article suggests that support groups can be very helpful, especially for those with rare conditions. It mentions that websites for support groups provide information and a network for individuals with dwarfism or specific related conditions, particularly in the UK.
Weiterführende Literatur und Referenzen
- Jain M, Saber AY; Dwarfism.
- Leiva-Gea A, Martos Lirio MF, Barreda Bonis AC, et al; Achondroplasie: Aktualisierung zu Diagnose, Nachsorge und Behandlung. An Pediatr (Engl Ed). 2022 Dez;97(6):423.e1-423.e11. doi: 10.1016/j.anpede.2022.10.004. Epub 2022 Nov 5.
- Ireland PJ, Pacey V, Zankl A, et al; Optimal management of complications associated with achondroplasia. Appl Clin Genet. 2014 Jun 24;7:117-25. doi: 10.2147/TACG.S51485. eCollection 2014.
- Vereinigung für eingeschränktes Wachstum (RGA) UK; Website einer eingetragenen Wohltätigkeitsorganisation, die Informationen und Unterstützung für Menschen mit Kleinwuchs und ihre Familien bietet.
- Types of Dwarfism; Little People UK
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About the authorView full bio

Dr Hayley Willacy, FRCGP
Allgemeinmediziner, Medizinischer Autor
MBChB (1992), DRCOG, DFFP, MRCOG (Part 1) MRCGP (2007), DFSRH (2013), MSc - medical education (2020)
Dr Hayley Willacy was an NHS GP working in northwest England, who retired from clinical practice in 2022 after 30 years.
About the reviewerView full bio

Dr Colin Tidy, MRCGP
Allgemeinmediziner, Medizinischer Autor
MBBS, MRCGP, MRCP (Paediatrics), DCH
Dr. Colin Tidy ist ein NHS-Arzt mit Sitz in Oxfordshire.
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