Prader Willi Syndrome (pws) – Complex Genetic Disorder Affecting Appetite

Willi Prader Syndrome occurs in approximately one of every 15,000 people. Willi prader syndrome is caused by a lack of active genetic substance in a particular region of chromosome 15. These genetic changes occurs in early embryonic development. Dysfunction of hypothalamus leads to Prader-Willi syndrome. Hypothalamus is a small endocrine organ in the brain that controls many function of the body.


Symptoms of Prader Willi Syndrome

  • A feeble, shrill cry in infancy
  • Infants is not able to drink from a bottle because of weak muscles
  • Mild cerebral retardation and learning disabilities
  • Bad temper, stubbornness, and unmanageable behavior.
  • Reduced motor skills
  • Rapid weight gain
  • A narrow
    face, almond-shaped eyes
  • Have surprisingly fair skin and light-colored hair
  • Underdeveloped gender organs
  • Short physique
  • Very small hands and feet in relationship to body
  • Poor muscle tone
  • Puberty is delayed or incomplete
  • Sleep disorders.
  • Strabismus,
  • Scoliosis
  • Osteoporosis
  • Bed-wetting
  • Dental problems
  • Type 2 diabetes
  • High blood pressure
  • Heart failure
  • Skin picking
  • Low to normal IQ
  • High threshold for pain
  • Insensitiveness to temperature extremes
  • Poor reflexes
  • Unquenchable desire for food


Treatment for Willy Syndrome

  • DNA-based Methylation-specific testing confirms the diagnosis of PWS. There is no treatment for Willy PraderSyndrome. Still, the physical problems caused by the syndrome can be managed as mentioned below
  • Special nipples for feedings are required until muscles become stronger.
  • Physical therapy and exercise helps improve muscle strength and coordination.
  • Hormonal and surgical treatments can be considered if testicles remain inside the abdominal area instead of dropping down.
  • Growth hormone replacement therapy to normalize height
  • Evaluation and treatment of
    sleep disturbance
  • Speech therapy can help children who are behind in their language skills
  • Replacement of sex hormones at puberty produces adequate secondary sexual characteristics
  • Firm limit-setting to treat behavioral problems; serotonin reuptake inhibitors are helpful for most individuals
  • Weight control to avoid development of diabetes
  • Calcium supplementation to keep away from osteoporosis
  • Administering human growth hormone (Genotropin, Humatrope, Norditropin) improves muscle mass and growth
  • Infants should be observed for strabismus, height, weight, and BMI to help then to give appropriate exercise and diet.


Article Written By dak

dak is a blogger at Expertscolumn.com

Last updated on 29-07-2016 2K 0

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