Today is my youngest daughter’s third birthday. A day of joy did not take long to also become a nightmare. Something was wrong with her, based upon our experience of having two other children. She did not cry. She did not eat. She did not wake up. It was a heart breaking night when my wife and I were in the hospital discussing the fact that something was wrong, but we did not know what. Four months later a geneticist found the problem: Prader-Willi Syndrome.
There is not any awareness about this syndrome, so I use this blog for personal reasons on my daughter’s birthday. She is three years old today and she is doing well, exceeding doctor’s expectations, to the praise of God’s glory. Below is a short idea of what Prader-Willi Syndrome (PWS) is and the links to find out more.
From the PWSA USA site:
What is Prader-Willi Syndrome?
- A disorder ofÂ chromosome 15
- Prevalence: 1:12,000- 15,000 (both sexes, all races)
- Major characteristics: hypotonia, hypogonadism,Â hyperphagia, cognitive impairment, difficult behaviors
- Major medical concern: morbid obesity
Cause and Diagnosis of PWS
The genetic cause is loss of yet unidentified genes normally contributedÂ by the father. Occurs from three main genetic errors: Approximately 70%Â of cases have a non-inherited deletion in the paternally contributedÂ chromosome 15; approximately 25% have maternal uniparental disomyÂ (UPD)–two maternal 15s and no paternalÂ chromosome 15; and 2—5 %Â have an error in the “imprinting” process that renders the paternalÂ contribution nonfunctional.
Weight and Behavior
Hypothalamic dysfunction is thought to be the cause of the disordered appetite/satiety function characteristic of PWS. Compulsive eating and obsession with food usually begin before age 6. The urge to eat is physiological and overwhelming; it is difficult to control and requires constant vigilance.
Weight Management Challenge
Compounding the pressure of excessive appetite is a decreased calorie utilization in those with PWS (typically 1,000-1,200 kcal per day for adults), due to low muscle mass and inactivity. A balanced, low-calorie diet with vitamin and calcium supplementation is recommended. Regular weigh-ins and periodic diet review are needed. The best meal and snack plan is one the family or caregiver is able to apply routinely and consistently. Weight control depends on external food restriction and may require locking the kitchen and food storage areas. Daily exercise (at least 30 minutes) also is essential for weight control and health.
To date, no medication or surgical intervention has been found that would eliminate the need for strict dieting and supervision around food. GH treatment, because it increases muscle mass and function, may allow a higher daily calorie level.
Infants and young children with PWS are typically happy and loving, and exhibit few behavior problems. Most older children and adults with PWS, however, do have difficulties with behavior regulation, manifested as difficulties with transitions and unanticipated changes. Onset of behavioral symptoms usually coincides with onset of hyperphagia (although not all problem behaviors are food-related), and difficulties peak in adolescence or early adulthood. Daily routines and structure, firm rules and limits, “time out,” and positive rewards work best for behavior management. Psychotropic medications–particularly serotonin reuptake inhibitors, such as fluoxetine and sertroline–are beneficial in treating obsessive-compulsive (OCD) symptoms, perseveration, and mood swings. Depression in adults is not uncommon. Psychotic episodes occur rarely.
Motor milestones are typically delayed one to two years; although hypotonia improves, deficits in strength, coordination, balance, and motor planning may continue. Physical and occupational therapies help promote skill development and proper function. Foot orthoses may be needed. Growth hormone treatment, by increasing muscle mass, may improve motor skills. Exercise and sports activities should be encouraged and adaptations made, as needed. Proficiency with jigsaw puzzles is frequently reported, reflecting strong visual-perceptual skills.
Oral Motor and Speech
Hypotonia may create feeding problems, poor oral-motor skills, and delayed speech. The need for speech therapy should be assessed in infancy. Sign language and picture communication boards can be used to reduce frustration and aid communication. Products to increase saliva may help articulation problems. Social skills training can improve pragmatic language use. Even with delays, verbal ability often becomes an area of strength for children with PWS. In rare cases, speech is severely affected.
IQs range from 40 to 105, with an average of 70. Those with normal IQs typically have learning disabilities. Problem areas may include attention, short-term auditory memory, and abstract thinking. Common strengths include long-term memory, reading ability, and receptive language. Early infant stimulation should be encouraged and the need for special education services and supports assessed in preschool and beyond.
Failure to thrive in infancy may necessitate tube feeding. Infants should be closely monitored for adequate calorie intake and appropriate weight gain. Growth hormone is typically deficient, causing short stature, lack of pubertal growth spurt, and a high body fat ratio, even in those with normal weight. The need for GH therapy should be assessed in both children and adults.
Sex hormone levels (testosterone and estrogen) are typically low. Cryptorchidism in male infants may require surgery. Both sexes have good response to treatment for hormone deficiencies, although side effects have been reported. Early pubic hair is common, but puberty is usually late in onset and incomplete.
Although it is often assumed that individuals with PWS are infertile, several pregnancies have been confirmed.
Â Other Common Concerns
- Strabismus–esotropia is common; requires early intervention, possibly surgery
- Scoliosis–can occur unusually early; may be difficult to detect withoutÂ X-ray; curve may progress with GH treatment. Kyphosis is also common in teens and adults
- Osteoporosis–can occur much earlier than usual and may causeÂ fractures; ensure adequate calcium, vitamin D, and weight-bearing exercise; bone density test recommended
- Diabetes mellitus, type II–secondary to obesity; responds well toÂ weight loss; screen obese patients regularly
- Other obesity-related problems–include hypoventilation, hypertension, right-sided heart failure, stasis ulcers, cellulitis, and skin problemsÂ in fat folds
- Sleep disturbances–hypoventilation and desaturation during sleep are common, as is daytime sleepiness; sleep apnea may develop with orÂ without obesity; sleep studies may be needed
- Nighttime enuresis–common at all ages; desmopressin acetate should be used in lower than normal doses
- Skin picking–a common, sometimes severe habit; usually in response to an existing lesion or itch on face, arms, legs, or rectum. BestÂ managed by ignoring behavior, treating and bandaging sores,Â and providing substitute activities for the hands.
- Dental problems–may include soft tooth enamel, thick sticky saliva,Â poor oral hygiene, teeth grinding, and infrequently rumination.Â Special toothbrushes can improve hygiene. Products to increaseÂ saliva flow are helpful.
Quality of Life Issues
General health is usually good in individuals with PWS. If weight is controlled, life expectancy may be normal, and the individual’s health and functioning can be maximized.
The constant need for food restriction and behavior management may be stressful for family members. PWSA (USA) can provide information and support. Family counseling may also be needed.
Adolescents and adults with PWS can function well in group and supported living programs, if the necessary diet control and structured environment are provided. Employment in sheltered workshops and other highly structured and supervised settings is successful for many. Residential and vocational providers must be fully informed regarding management of PWS.