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Health What Is Prader-Willi Syndrome? This 380-Pound Pageant Queen Has a Condition That Makes Her Hungry All the Time

21:11  29 march  2018
21:11  29 march  2018 Source:   msn.com

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This 380 - Pound Pageant Queen Has a Condition That Makes Her Hungry All the Time . People with Prader - Willi syndrome often live with health complications due to their weight. Hankins, for example, is so obese that she cannot dress herself, and she requires supplemental oxygen to help

This 380 - Pound Pageant Queen Has a Condition That Makes Her Hungry All the Time . People with Prader - Willi syndrome often live with health complications due to their weight. Hankins, for example, is so obese that she cannot dress herself, and she requires supplemental oxygen to help

  What Is Prader-Willi Syndrome? This 380-Pound Pageant Queen Has a Condition That Makes Her Hungry All the Time © Provided by TIME Inc.

Anna Hankins isn’t letting her genetic condition stop her from living life: The 15-year-old with Prader-Willi syndrome was recently crowned Mississippi Miss Amazing, and now her inspiring story is going viral.

Prader-Willi syndrome is a genetic condition that causes constant hunger and chronic overeating. According to British news service SWNS, Hankins’ insatiable appetite started around age 2, and she now weighs 380 pounds.

"When she was little, the first words out of her mouth were ‘I’m hungry’ and the last ones were 'I'm hungry,'" Hankins’ mother told SWNS. Hankins’ family used to find empty food and candy wrappers in her room and resorted to locking the refrigerator. "We just didn’t know how to stop it,” her mother added. “She got bigger and bigger and bigger."

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380 - Pound Girl With Rare Condition Crowned Pageant Queen . The family later found that she was suffering from Prader - Willi Syndrome , a condition that affects one in 15,000 babies born in the This is a rare genetic condition that causes obesity as the patient has constant urges to eat food.

Prader – Willi syndrome (PWS) is a genetic disorder due to loss of function of specific genes. In newborns symptoms include weak muscles, poor feeding, and slow development.

After Hankins was crowned a pageant queen for the Mississippi chapter of Miss Amazing—an organization that recognizes girls with disabilities—her story was picked up by news outlets around the world.

To learn more about this condition, Health spoke with Jessica Duis, MD, assistant professor of pediatrics and director of the Prader-Willi Syndrome Clinic at Vanderbilt University’s Monroe Children’s Hospital. Dr. Duis has not treated Hankins, but here’s what she wants people to know about children—and adults—with this condition.

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For starters, Prader-Willi syndrome is rare: It affects about one in every 15,000 babies born in the United States. It’s caused by a genetic defect that usually happens around the time of conception–and not by anything that either parent has control over.

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A 380 - pound girl with a rare condition that causes her to constantly be hungry was crowned a pageant queen in Mississippi. Anna Hankins, 15, suffers from Prader - Willi Syndrome , an incurable genetic disorder in which patients develop an insatiable appetite, leading to chronic overeating and

Anna Hankins won't let anything get between her and her lust for life. The 15-year-old has a genetic condition called Prader - Willi Syndrome , which causes

According to SWNS, Hankins’ parents didn’t know how to treat her condition when she was young, and they allowed her to overeat. When she was 14, a Prader-Willi specialist put her on a 900-calorie-a-day diet that includes vegetables, meat, rice, fruit, and vitamin supplements.

Despite those restrictions, Hankins still hasn’t lost weight. That’s a common problem for people with Prader-Willi syndrome, says Dr. Duis, as their metabolisms are slower than people without the condition.

People with Prader-Willi syndrome often live with health complications due to their weight. Hankins, for example, is so obese that she cannot dress herself, and she requires supplemental oxygen to help her breathe. “It can be difficult to deal with sometimes,” she told SWNS.

Some signs of Prader-Willi syndrome can be present even at birth. Babies with this condition sometimes have poor muscle tone. “We describe them as kind of 'floppy' as infants,” says Dr. Duis.

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At 380 pounds , Hankins suffers from Prader - Willi syndrome (PWS), an unusual genetic disorder that leaves her constantly hungry . “She eats anything she can get.” Prader - Willi syndrome is a debilitating condition that occurs in roughly 1 out of every 15,000 births.

“She is hungry all the time ,” her mother said. A 380 - pound beauty queen wants to bring attention to a rare disorder that causes constant hunger . She said that Anna’s condition prevents her from participating in sports and other extracurricular activities, but the annual pageant gives her something to do. “ Prader - Willi syndrome is rare, but Anna takes those difficulties in stride,” Brasfield said in

Babies with Prader-Willi syndrome can also have distinct facial features—like almond-shaped eyes, a turned-down mouth, and a thin upper lip. It’s also common for them to have a poor sucking reflex, and they may seem tired, weak, unresponsive, and uninterested in eating too.

Toddlers with Prader-Willi syndrome may start walking or speaking later than other children. Eventually, their appetite increases, and usually by 8 years old, they begin showing signs of unrelenting hunger. “They have a genetic drive to eat, and they have no ability to feel full,” says Dr. Duis.

These children may develop strange behaviors around food, like hoarding or even eating garbage. “Parents sometimes think it’s a moral issue, because they catch their kids stealing food,” says Dr. Duis. They can also develop other obsessive-compulsive or repetitive behaviors, along with anxiety.

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Hypogonadism, a condition in which the body produces little or no sex hormones, is also common in people with Prader-Willi syndrome. This means they can have underdeveloped sex organs and delayed puberty, and they can almost never have children of their own. Intellectual and learning disabilities are also common among people with Prader-Willi syndrome.

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Playing 380 - Pound Teen With 'Chronic Eating' Condition Wins Pageant Crown. A Mississippi 15-year-old girl who weighs 380 pounds due to a rare condition that causes incessant hunger has been crowned a pageant queen . Anna Hankins has Prader - Willi Syndrome , a rare and incurable "It's a moment where we can forget about all her problems." What is Prader - Willi Syndrome ?

Prader - Willi syndrome is a complex genetic condition that affects many parts of the body. In infancy, this condition is characterized by weak muscle tone Among these are genes that provide instructions for making molecules called small nucleolar RNAs (snoRNAs). These molecules have a variety of

While there’s no cure for Prader-Willi syndrome, treating patients with growth hormones has been shown to improve the balance of fat and muscle in their bodies, as well as their verbal IQs. It also helps them grow taller, since many people with Prader-Willi syndrome are deficient in these hormones and, without intervention, end up with short stature.

Putting patients on a modified Atkins diet also helps prevent or reduce obesity, says Dr. Duis. “If you put kids on a very low-carbohydrate diet, where they’re just getting nutritious carbs like vegetables and whole grains, it actually modifies the natural history of the disease,” she says. “Now we start children on that diet very early on, and we can keep them from gaining weight. Even for adults with Prader-Willi, it can help with weight loss.”

Caregivers still have to count calories and pay close attention to food intake, though: “We recommend as soon as kids are in those early childhood years you introduce the concept of locking up the refrigerator and restricting access to food,” she says. “When we talk to teenagers who have grown up in that environment, it actually helps with their level of anxiety because they know they’re protected.”

There seems to be an increased risk of sudden death among infants and children with Prader-Willi syndrome, says Dr. Duis, although experts aren’t sure exactly why. But, she adds, if the condition is diagnosed and treated early, people with Prader-Willi syndrome can maintain a normal weight and have a normal life expectancy. They can also live very fulfilled lives, finishing school, holding jobs, and moving away from home as adults.

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A15-year-old girl, who weighs 380 lbs (172kg), suffers from a rare condition that makes her so the strict diet plan, Anna still tips the scales at 380 lbs.She said: 'I have Prader - Willi Syndrome and I get Prader - Willi Syndrome : A Full Life Without Limits - Продолжительность: 4:28 PWCFVIDEOS 2 249 просмотров. Girl with rare condition that makes her constantly hungry wins beauty pageant

Prader - Willi Syndrome (PWS) is a rare genetic disorder. It causes poor muscle tone, low levels of sex hormones and a constant feeling of hunger . The part of the brain that controls feelings of fullness or hunger does not work properly in people with PWS.

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There are other reasons for Prader-Willi patients and their family members to be hopeful as well, says Dr. Duis. “We’re a lot smarter than we were 20 years ago,” she says. "Plus, there are just so many clinical trials coming, and there’s a lot of interest from pharmacological companies.” she says.

Studies are currently looking at the role the hormones ghrelin and oxytocin play in Prader-Willi syndrome and whether changing those hormone levels can reduce symptoms like hunger and anxiety. “There’s so much coming down the pipeline," Dr. Duis says. "I think that—especially for younger kids—growing up with Prader-Willi syndrome will be completely different than it was for people who are adults now.”

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