rare genetic disorder

Prader–Willi syndrome (abbreviated PWS) is a rare genetic disorder in which seven genes (or some subset thereof) on chromosome 15 (q 11-13) are deleted or unexpressed (chromosome 15q partial deletion) on the paternal chromosome. It was first described in 1956 by Andrea Prader, Heinrich Willi, Alexis Labhart, Andrew Ziegler, and Guido Fanconi of Switzerland.[1] The incidence of PWS is between 1 in 10,000 and 1 in 25,000 live births. The paternal gene origin is lost due to deletion and the maternal genes are silenced due to imprinting. PWS has the sister syndrome Angelman syndrome that includes maternally deleted and paternally imprinted genes in the same genetic region.
Contents [hide]
1 Signs and symptoms
1.1 Neuro-cognitive
1.2 Behavioral
1.3 Endocrine
2 Genetics
3 Diagnosis
3.1 Differential diagnosis
4 Treatment
5 Society and culture
6 See also
7 References
8 External links
[edit]Signs and symptoms



patient with the syndrome, showing characteristic facial appearance, with elongated face, prominent nose, and smooth philtrum
Clinical features and signs
Holm et al. (1993) describe the following features and signs as pretest indicators of PWS, although not all will be present.
In utero:
Reduced fetal movement
Frequent abnormal fetal position
Occasional polyhydramnios (excessive amniotic fluid)
At birth:
Often breech or caesarean births
Lethargy
Hypotonia
Feeding difficulties (due to poor muscle tone affecting sucking reflex)
Difficulties establishing respiration
Hypogonadism
Infancy:
Failure to thrive (continued feeding difficulties)
Delayed milestones/intellectual delay
Excessive sleeping
Strabismus
Scoliosis (often not detected at birth)
Childhood:
Speech delay
Poor physical coordination
Hyperphagia (over-eating) from age 2 – 8 years. Note change from feeding difficulties in infancy
Excessive weight gain
Sleep disorders
Scoliosis
Adolescence:
Delayed puberty
Short stature
Obesity
Extremely flexible
Adulthood:
Infertility (males and females)
Hypogonadism
Sparse pubic hair
Obesity
Hypotonia
Learning disabilities/borderline intellectual functioning (but some cases of average intelligence)
Prone to diabetes mellitus
Extreme flexibility.
General physical appearance (adults)
Prominent nasal bridge
Small hands and feet with tapering of fingers
Soft skin, which is easily bruised
Excess fat, especially in the central portion of the body
High, narrow forehead
Almond shaped eyes with thin, down-turned lips
Light skin and hair relative to other family members
Lack of complete sexual development
Frequent skin picking
Striae
Delayed motor development
[edit]Neuro-cognitive
Individuals with PWS are at risk of learning and attention difficulties. Curfs and Frym (1992) conducted research into the varying degrees of learning disability found in Prader Willi Syndrome (PWS).[2] Their results were as follows:
5%: IQ above 85 (average to low average intelligence)
27%: IQ 70 – 85 (borderline intellectual functioning)
39%: IQ 50 – 70 (mild intellectual disability)
27%: IQ 35 – 50 (moderate intellectual disability)
1%: IQ 20 – 35 (severe intellectual disability)
<1%: IQ <20 (profound intellectual disability)
Cassidy found that 40% of individuals with PWS have borderline/low average intelligence,[3] a figure higher than that found in Curfs and Frym's study (32%).[2] However, both studies suggest that most individuals (50% – 65%) fall within the mild/borderline/low average intelligence range.
Children with PWS show an unusual cognitive profile. They are often strong in visual organization and perception, including reading and vocabulary, but their spoken language (sometimes affected by hypernasality) is generally poorer than their comprehension. A marked skill in completing jigsaw puzzles has been noted.[4][5]
Auditory information processing and sequential processing are relatively poor, as are arithmetic and writing skills, visual and auditory short term memory and auditory attention span. These sometimes improve with age, but deficits in these areas remain throughout adulthood.[4]
[edit]Behavioral
Prader–Willi syndrome is also frequently associated with an extreme and insatiable appetite, often resulting in morbid obesity. There is currently no consensus as to the cause for this particular symptom, although genetic abnormalities in chromosome 15 disrupt the normal functioning of the hypothalamus.[3] Given that the hypothalamus regulates many basic processes, including appetite, there may well be a link. However, no organic defect of the hypothalamus has been discovered on post mortem investigation.[3]
Prader–Willi syndrome patients have high ghrelin levels, which are thought to directly contribute to the increased appetite, hyperphagia, and obesity seen in this syndrome. Cassidy states the need for a clear delineation of behavioural expectations, the reinforcement of behavioural limits and the establishment of regular routines.[21]
The main mental health difficulties experienced by people with PWS include compulsive behaviour (usually manifested in skin-picking) and anxiety (Udwin, 1998; Clark et al., 1995). Psychiatric symptoms, for example, hallucinations, paranoia and depression have been described in some cases (Udwin, 1998) and affect approximately 5 - 10% of young adults (Cassidy, 1997). Psychiatric and behavioural problems are the most common cause of hospitalization (Cassidy et al., 1994).
[edit]Endocrine
There are several aspects of PWS that support the concept of growth hormone deficiency in individuals with PWS. Specifically, individuals with PWS have short stature, are obese with abnormal body composition, have reduced fat free mass (FFM), have reduced LBM and total energy expenditure, and have decreased bone density.
PWS is characterized by hypogonadism. This is manifested as undescended testes in males and benign premature adrenarche in females. Testes may descend with time or can be managed with surgery or testosterone replacement. Adrenarche may be treated with hormone replacement therapy.
[edit]Genetics


PWS is caused by the deletion of the paternal copies of the imprinted SNRPN and necdin genes along with clusters of snoRNAs: SNORD64, SNORD107, SNORD108 and two copies of SNORD109, 29 copies of SNORD116 (HBII-85) and 48 copies of SNORD115 (HBII-52). These are on chromosome 15 located in the region 15q11-13.[6][7][8] This so-called PWS/AS region may be lost by one of several genetic mechanisms which, in the majority of instances occurs through chance mutation. Other less common mechanisms include; uniparental disomy, sporadic mutations, chromosome translocations, and gene deletions. Due to imprinting, the maternally inherited copies of these genes are virtually silent, only the paternal copies of the genes are expressed. PWS results from the loss of paternal copies of this region. Deletion of the same region on the maternal chromosome causes Angelman syndrome (AS). PWS and AS represent the first reported instances of imprinting disorders in humans.
The risk to the sibling of an affected child of having PWS depends upon the genetic mechanism which caused the disorder. The risk to siblings is <1% if the affected child has a gene deletion or uniparental disomy, up to 50% if the affected child has a mutation of the imprinting control region, and up to 25% if a parental chromosomal translocation is present. Prenatal testing is possible for any of the known genetic mechanisms.
A microdeletion in one family of the snoRNA HBII-52 has excluded it from playing a major role in the disease.[9]
Studies of human and mouse model systems have shown that deletion of the 29 copies of the C/D box snoRNA SNORD116 (HBII-85) has been shown to be the primary cause of Prader–Willi syndrome.[10][11][12][13] [14]
[edit]Diagnosis



Prader-Willi syndrome phenotype at 15 years of age. Note absence of typical PWS facial features and presence of mild truncal obesity.
PWS affects approximately 1 in 10,000 to 1 in 25,000 newborns.[15] There are more than 400,000 people who live with PWS around the world.[16] It is traditionally characterized by hypotonia, short stature, hyperphagia, obesity, behavioral issues (specifically OCD-like behaviors), small hands and feet, hypogonadism, and mild mental retardation.[15] However, with early diagnosis and early treatment (such as with growth hormone therapy), the prognosis for persons with PWS is beginning to change. Like autism, PWS is a spectrum disorder and so symptoms can range from mild to severe, and may change throughout the person's lifetime. Various organ systems are affected.
Traditionally, Prader-Willi Syndrome was diagnosed by clinical presentation. Currently, the syndrome is diagnosed through genetic testing; testing is recommended for newborns with pronounced hypotonia. Early diagnosis of PWS allows for early intervention as well as the early prescription of growth hormone. Daily recombinant growth hormone (GH) injections are indicated for children with PWS. GH supports linear growth and increased muscle mass, and may lessen food preoccupation and weight gain.
The mainstay of diagnosis is genetic testing, specifically DNA-based methylation testing to detect the absence of the paternally contributed Prader–Willi syndrome/Angelman syndrome (PWS/AS) region on chromosome 15q11-q13. Such testing detects over 97% of patients. Methylation-specific testing is important to confirm the diagnosis of PWS in all individuals, but especially those who are too young to manifest sufficient features to make the diagnosis on clinical grounds or in those individuals who have atypical findings. Because PWS infants have a higher rate of difficulties at birth (including breech delivery and respiratory delay) birth-related injuries and oxygen deprivation may complicate the genetic handicaps, resulting in atypical PWS.[citation needed]
[edit]Differential diagnosis
Prader–Willi syndrome is often misdiagnosed as a variety of other syndromes due to many in the medical community's unfamiliarity with PWS. Sometimes it is misdiagnosed as Down syndrome, simply because of the relative frequency of Down syndrome compared to PWS. Also, marked obesity can occur in Down syndrome due to behavioral problems. Adding to the confusion, parents of children who already carry a diagnosis of Prader–Willi syndrome may tell friends, family, and even physicians and nurses that their child has Down syndrome because more people have heard of that condition.[citation needed] It is thought that 75% of those with PWS are undiagnosed.
[edit]Treatment

Prader–Willi syndrome has no cure, however, several treatments are in place to lessen the condition's symptoms. During infancy, subjects should undergo therapies to improve muscle tone. Speech and occupational therapy are also indicated. During the school years, children benefit from a highly structured learning environment as well as extra help. The largest problem associated with the syndrome is severe obesity.
Prescription of daily recombinant growth hormone injections are indicated for children with PWS. GH supports linear growth and increased muscle mass, and may lessen food preoccupation and weight gain.[17][18][19]
Because of severe obesity, obstructive sleep apnea is a common sequela, and a positive airway pressure machine is often needed.
[edit]Society and culture

Prader–Willi syndrome appeared in the UK media in July 2007 when Channel 4 aired a program Can't Stop Eating, surrounding the everyday lives of two Prader-Willi patients, Joe and Tamara.[20]
A sufferer from Prader-Willi Syndrome featured in the episode entitled 'Dog Eat Dog' of the television series CSI: Crime Scene Investigation (aired on November 24, 2005).[21]
Another sufferer Ethan Starkweather was on Extreme Makeover: Home Edition originally aired on Mothers Day 2010.