Prader-Willi Syndrome

oPatientPlus articles are written by UK doctors and are based on research evidence, UK and European Guidelines. They are designed for health professionals to use, so you may find the language more technical than the condition leaflets.

Prader-Willi syndrome (PWS) is a complex genetic disorder characterised by hypotonia and developmental delay as an infant and obesity, learning disability and behaviour problems (especially relating to food) in adolescence and adulthood.

Prader-Willi syndrome (PWS) was the first human disorder attributed to genomic imprinting.[1]

  • It is an autosomal dominant disorder that is caused by:[2]
  • Deletion of the paternally inherited chromosomal 15q11.2-q13 region (occasionally a result of translocation.) These are the majority.
  • Maternal uniparental disomy 15 caused by chromosomal nondisjunction (both copies are from the mother).
  • A defect in the imprinting process in the 15q11.2-q13 region on the paternally inherited chromosome.

The opposite, ie maternal deletion or paternal uniparental disomy, causes Angelman's syndrome.

It is relatively common - prevalence 1/15,000-1/30,000.[2] Despite the genetic cause it appears to be sporadic rather than inherited in a Mendelian pattern. Sex ratio is equal and it occurs in all races.

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As diagnostic testing is now available these should serve to raise suspicion and ensure that all appropriate people are tested but avoid the expense and worry of unnecessary testing.[3]

  • From birth to age 3 requires 5 points including 4 major criteria.
  • Age 3 to adult requires 8 total points including 5 major criteria.

Major criteria (1 point each):

  • Neonatal or infantile central hypotonia with a poor suck. This gradually improves with age.
  • Feeding problems in infancy or failure to thrive.
  • Excessive weight gain between 1 and 6 years of age. Morphological and hormonal abnormalities of the pituitary gland are found in Prader-Willi syndrome (PWS).[4] Marked differences in obesity have been found between patients living in different countries. It is thought that these differences could be explained by differences in management.[5]
  • Characteristic facial features (narrow face, almond-shaped eyes, etc.).
  • Hypogonadism - genital hypoplasia and/or delayed or incomplete gonadal maturation (this is not always associated with infertility in boys).[6]
  • Cryptorchidism is common.
  • Global developmental delay (in child aged <6 years). They may not sit until 12 months, or walk until 24 months. Older children show mild-to-moderate learning difficulties and an IQ of 50 to 70.
  • Hyperphagia with excessive appetite or food obsession.
  • Chromosomal abnormality - deletion 15q 11-13 or other appropriate molecular abnormality in this chromosomal region.

Minor criteria (0.5 points each):

  • Decreased fetal movements, infantile lethargy or weak cry in infancy, which improves with age.
  • Characteristic behavioural problems (typically tantrums or obsessive/compulsive behaviour).[7] Adults may have psychotic episodes.
  • Sleep disturbance/sleep apnoea .
  • Short stature in childhood and failure of pubertal growth spurt.
  • Hypopigmentation - fair skin and hair.
  • Small hands and feet.
  • Narrow hands with straight ulnar border.
  • Eye abnormalities (esotropia, myopia).
  • Thick, viscous saliva ± crusting at mouth corners.
  • Speech articulation defects.
  • Skin picking.

Other features which may be present, many of them related to problems of the hypothalamus:

  • High pain threshold.
  • Decreased vomiting.
  • Temperature instability or altered temperature sensitivity.
  • Scoliosis or kyphosis (66.7% at skeletal maturity in one series of 145 patients).[8]
  • Early adrenarche (pubic or axillary hair before age 8) despite retardation of other sexual development.
  • Obesity may cause type 2 diabetes at an early age, also called 'maturity onset diabetes of the young' (MODY).
  • Osteoporosis (because of hypogonadism). Along with a high pain threshold this can lead to pathological fractures that are not instantly recognised.
  • They display an unusual skill with jigsaw puzzles.[9]
  • IQ is usually in the range of 60 to 80 but with expected individual variation. Genetic subtypes of the condition have differing IQ strengths - verbal vs performance IQ.[10]

PWS patients have a different gait from individuals who are simply obese.[11]

This may be seen as a disease in two stages:

  • After birth there is hypotonia, failure to thrive and sleepiness. The child usually has blue eyes and blond hair. They tend to lag behind other children in the transition to solid food.
  • The second stage becomes apparent at the age of 12-18 months, when an exceptional interest in food becomes apparent.[7] Hyperphagia, obesity, hypogonadism, short stature and sleep apnoea and cor pulmonale occur.[12] They have markedly elevated levels of ghrelin, a hormone associated with hunger.[13]

DNA methylation analysis and fluorescent in situ hybridisation (FISH) techniques can diagnose Prader-Willi syndrome (PWS) in all three types of PWS, as well as differentiate PWS from Angelman's syndrome in deletion cases.[2]
Other tests:

  • If the patient is obese, screening for glucose intolerance is advised.
  • Endocrine studies include insulin-like growth factor, lipids and thyroid function. LDL tends to be high and HDL low.
  • Body composition analysis by dual-energy X-ray absorptiometry (DEXA), anthropometry or another method. DEXA is used to assess fat mass rather than bone mineral density in this case.
  • Psychological and/or educational testing.

A multidisciplinary approach is essential:

  • Family support is essential to cope with the behavioural difficulties throughout childhood. The child must be kept away from food and subsequent obesity. Their energy requirements are only about 75% of that of a normal child and hyperphagia can occasionally be dangerous, causing massive stomach dilation. Regular exercise is important.
  • Input from a paediatric gastroenterologist, endocrinologist, psychologist, psychiatrist, dietitian, occupational therapists, speech therapists, exercise advisors and orthopaedic consultants may be helpful. Bariatric surgery has had poor results compared with normal, obese adolescents.[14]
  • Management of the transition period from childhood to adulthood is important and placement in a residential home may need to be considered.[15] The GP will continue to provide care throughout the transition and during adulthood. Specific points related to Prader-Willi syndrome (PWS) to consider during a health check include:
    • Sleep apnoea (obstructive, central or mixed) - even where obesity is not a problem.
    • Scoliosis, kyphosis.
    • Osteoporosis.
    • Oedema.
    • Cellulitis.
    • Hypothyroidism.
    • Gastroparesis.
    • Type 2 diabetes.
    • Skin infections (consequence of skin-picking).
    • Squint, myopia.

Pharmacological

  • Growth hormone is essential to maintain normal growth, muscle development and avoid obesity.[12][16] One study found that growth hormone also improved behavioural difficulties.[17] Growth hormone treatment was initially thought to make scoliosis worse but this has been refuted.[18]
  • Appetite suppressant drugs are of no value. Long-acting octreotide reduces ghrelin secretion but does not affect behaviour or weight.[19]
  • Many drugs have been used to modify behaviour but they tend to be ineffective or even counterproductive. Olanzapine may have an effect.
  • Haloperidol and fluoxetine are sometimes effective.
  • Selective serotonin reuptake inhibitors (SSRIs) seem to have a nonspecific behaviour-stabilising effect, with fewer outbursts, a marked reduction in irritability and less perseveration but with no antidepressant effect.
  • All these drugs may be tried with care. None are universally successful and they may even be counterproductive.

Recurrence risk depends on the mechanism causing Prader-Willi syndrome (PWS) in the individual:[20]

  • Deletion is sporadic and has a recurrence rate of ≤1% (except in the rare cases where a chromosomal rearrangement is present in the father).
  • Maternal uniparental disomy 15 is typically de novo also with a recurrence rate of ≤1% (except if a Robertsonian translocation is present in either parent).
  • A proportion of those with an imprinting defect have a microdeletion in the imprinting centre; this can be familial and has a 50% recurrence risk when it is. However, the greater proportion of those with an imprinting defect have an epigenetic mutation and the recurrence risk is ≤1% for this group.

Obesity-related cardiovascular and respiratory disorders are the most frequent causes of death in both children and adults. Based on a population study, the death rate has been estimated at 3% per year.[20]

Further reading & references

  1. Cassidy SB, Schwartz S; Prader-Willi and Angelman syndromes. Disorders of genomic imprinting. Medicine (Baltimore). 1998 Mar;77(2):140-51.
  2. Cassidy SB, Driscoll DJ; Prader-Willi syndrome. Eur J Hum Genet. 2009 Jan;17(1):3-13. Epub 2008 Sep 10.
  3. Gunay-Aygun M, Schwartz S, Heeger S, et al; The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and Pediatrics. 2001 Nov;108(5):E92.
  4. Miller JL, Goldstone AP, Couch JA, et al; Pituitary abnormalities in Prader-Willi syndrome and early onset morbid obesity. Am J Med Genet A. 2008 Mar 1;146A(5):570-7.
  5. Dudley O, McManus B, Vogels A, et al; Cross-cultural comparisons of obesity and growth in Prader-Willi syndrome. J Intellect Disabil Res. 2008 May;52(Pt 5):426-36. Epub 2008 Feb 20.
  6. Vogels A, Moerman P, Frijns JP, et al; Testicular histology in boys with Prader-Willi syndrome: fertile or infertile? J Urol. 2008 Oct;180(4 Suppl):1800-4. Epub 2008 Aug 21.
  7. Prader-Willi Syndrome, Online Mendelian Inheritance in Man (OMIM)
  8. Odent T, Accadbled F, Koureas G, et al; Scoliosis in patients with Prader-Willi Syndrome. Pediatrics. 2008 Aug;122(2):e499-503. Epub 2008 Jul 7.
  9. Verdine BN, Troseth GL, Hodapp RM, et al; Strategies and correlates of jigsaw puzzle and visuospatial performance by persons with Prader-Willi syndrome. Am J Ment Retard. 2008 Sep;113(5):343-55.
  10. Whittington J, Holland A, Webb T; Relationship between the IQ of people with Prader-Willi syndrome and that of their siblings: evidence for imprinted gene effects. J Intellect Disabil Res. 2009 Feb 4.
  11. Vismara L, Romei M, Galli M, et al; Clinical implications of gait analysis in the rehabilitation of adult patients with "Prader-Willi" Syndrome: a cross-sectional comparative study ("Prader-Willi" Syndrome vs matched obese patients and healthy subjects). J Neuroeng Rehabil. 2007 May 10;4:14.
  12. Couper RT, Couper JJ; Prader-Willi syndrome. Lancet. 2000 Aug 19;356(9230):673-5.
  13. Hauffa BP, Haase K, Range IM, et al; The Effect of Growth Hormone on the Response of Total and Acylated Ghrelin to a Standardized Oral Glucose Load, and Insulin Resistance in Children with Prader-Willi Syndrome. J Clin Endocrinol Metab. 2006 Dec 27;.
  14. Scheimann AO, Butler MG, Gourash L, et al; Critical analysis of bariatric procedures in Prader-Willi syndrome. J Pediatr Gastroenterol Nutr. 2008 Jan;46(1):80-3.
  15. Goldstone AP, Holland AJ, Hauffa BP, et al; Recommendations for the diagnosis and management of Prader-Willi syndrome. J Clin Endocrinol Metab. 2008 Nov;93(11):4183-97. Epub 2008 Aug 12.
  16. Kirk J; Indications for GH therapy in children. Arch Dis Child. 2011 May 3.
  17. Whitman BY, Myers S, Carrel A, et al; The behavioral impact of growth hormone treatment for children and adolescents with Prader-Willi syndrome: a 2-year, controlled study. Pediatrics. 2002 Feb;109(2):E35.
  18. de Lind van Wijngaarden RF, de Klerk LW, Festen DA, et al; Randomized controlled trial to investigate the effects of growth hormone treatment on scoliosis in children with Prader-Willi syndrome. J Clin Endocrinol Metab. 2009 Jan 21.
  19. De Waele K, Ishkanian SL, Bogarin R, et al; Long-acting octreotide treatment causes a sustained decrease in ghrelin Eur J Endocrinol. 2008 Oct;159(4):381-8. Epub 2008 Jul 4.
  20. Butler JV, Whittington JE, Holland AJ, et al; Prevalence of, and risk factors for, physical ill-health in people with Dev Med Child Neurol. 2002 Apr;44(4):248-55.

Disclaimer: This article is for information only and should not be used for the diagnosis or treatment of medical conditions. EMIS has used all reasonable care in compiling the information but make no warranty as to its accuracy. Consult a doctor or other health care professional for diagnosis and treatment of medical conditions. For details see our conditions.

Original Author:
Dr Laurence Knott
Current Version:
Peer Reviewer:
Dr Adrian Bonsall
Last Checked:
19/08/2011
Document ID:
2649 (v22)
© EMIS