There is no cure, but surgery can help. The story of August “Auggie” Pullman, who was born with a rare facial deformity called Treacher Collins Syndrome and a cleft palate. Jacob Tremblay und seine Familie trafen im Vorfeld … While the book and movie are … Sindrom Treacher Collins. Treacher Collins syndrome is usually a chronic respiratory failure accompanied by conductive hearing loss caused by deformation of the outer or middle ear apnea and insomnia. In some children the condition is almost unnoticeable, but in others, like Auggie, the symptoms are severe. It causes physical deformities of the ears, eyes, cheekbones, mouth, and chin which in turn can lead to having a cleft palate, and vision, breathing, and hearing loss. "Wonder Auggie’s Condition: Treacher Collins Syndrome (TCS)". It has no cure, but in no way affects the intellect of those who suffer from it, as many mistakenly think. Genes are the smallest units of hereditary information and may be thought of as a blueprint or "code" for everything that takes place in … The ears are frequently abnormal and part of the outer ear is usually absent. Luckily, most of the physical problems caused by Treacher Collins syndrome can be addressed with surgery, and the vast majority of patients go on to live long and happy lives. TCS is a condition in which the cheek-bones and jawbones are underdeveloped. The movie “Wonder,” based on the New York Times bestseller, premiered worldwide today, and although the movie is fictional, the storyline sheds light on a rare craniofacial condition affecting one in 50,000 newborns: Treacher Collins syndrome. Treacher Collins Syndrome Worksheets. It can cause physical deformity, hearing problems, and social challenges. That’s why it’s important patients and their families don’t just see doctors for their physical symptoms, says Dr. Hopper, but that they also talk to a social worker or therapist if their emotional health is suffering. • Treacher–Collins syndrome occurs as an autosomal-dominant disorder in 1 per 50 000 live births, 60% of cases arise as sporadic mutations. We're loving their inspirational, body-positive messages. Treacher Collins syndrome, also known as mandibulofacial dysostosis or Franceschetti-Zwahlen-Klein syndrome, is an autosomal dominant disorder caused by mutations in the TCOF1 gene mapped to chromosome 5q32-q33.1, which encodes a nucleolar phosphoprotein called treacle [2,3]. Check out this real-life Treacher Collins Syndrome wonder! Stay in your living room and still spike your heart rate. “Kids want to play sports and run around outside, but that can be challenging when you’re using a breathing tube or your eyes aren’t fully protected the way they should be,” says Dr. Hopper. The story features a young boy named August who has Treacher Collins syndrome. Both the Wonder book and Wonder movie provide fantastic study tools that cover so many different topics: bullying, differences, kindness, relationships, and more. Treacher Collins is an extremely rare … It’s the first time “Auggie” (played by Jacob Tremblay) has been to school outside of the home, because he was born with Treacher Collins syndrome, a rare facial deformity that’s required dozens of surgeries during his first decade of life. Health.com may receive compensation for some links to products and services on this website. But Auggie also makes friends and inspires those around him to look past his facial differences, see him for who he really is, and treat each other with kindness. They also usually have normally functioning bodies that develop just like other children their age. This is really looking for your opinion rather than mine. This engaging and informative lesson enables students to understand the role that the theme of ‘appearances’ plays in R.J. Palacio’s Wonder. Hallmarks of this syndrome are underdeveloped cheek bones, a small jaw and chin, a cleft palate, and eyes that slant downward. Ms. RJ Palacio wrote Wonder as a result of an encounter of her sons with a young child with Treacher Collins Syndrome in a Brooklyn ice cream parlor. Wonder Movie Trailer [VIDEO] If you haven’t seen the Wonder movie yet, grab a tissue because just the Wonder movie trailer will stab you right in the heart! Babies who have it are born with deformed ears, eyelids, cheek bones, and jawbones. He said the doctor flipped open a page showing a black and white photo of a teenager with Treacher Collins syndrome. Here are the ones you need to pay attention to, and how to know if you may have an anxiety disorder. Der englische Augenarzt Edward Treacher Collins beschrieb im Jahre 1900 erstmals das kombinierte Auftreten der charakteristischen Merkmale des … Treacher Collins syndrome is a craniofacial deformity, meaning that the bones and tissues of the face do not develop as they should. Treacher Collins syndrome, named for Edward Treacher Collins who first described its symptoms, is a rare congenital disorder that impacts facial features. He finds friends in Jack, Charlotte, and Summer, but he must learn to deal with bullying, betrayal, and misunderstandings. The treatment of Treacher-Collins syndrome is often lengthy and involves a multidiscipline approach that focuses on the treatment of symptoms. “Although the severity of the syndrome can vary from child to child, the facial characteristics of Treacher Collins syndrome are usually quite recognizable,” said Dr. Michael Cunningham , medical director of Seattle Children’s Craniofacial Center . ABC News' Elizabeth Vargas on being inspired by a boy with Treacher Collins and the book 'Wonder': Reporter's Notebook Elizabeth Vargas on the inspiring life of a boy living with Treacher Collins. Treacher Collins syndrome (TCS) is a rare condition. … Their mean spiritedness, however, really bothered him. The condition has been linked to certain gene mutations, and it can be passed from parent to child—but in about 60% of cases, the mutation arises spontaneously, meaning there is no family history and no known cause. Auggie experiences this last problem and eventually requires hearing aids in order to hear properly. (Isn’t that Wonder book cover fantastic?) I found out this fact, this diagnosis, while attempting sleep after 26 hours of hard labor and then hard surgery. Plastic surgery can help to normalize facial structure, and other procedures can be undertaken to correct jaw problems, cleft palates, and other facial abnormalities. As I mentioned in a post last month, I’ve decided to branch out beyond telling only our tale and instead feature some of the amazing families I’ve been lucky enough to connect with whose children have Treacher Collins Syndrome (TCS). In 2017, a film adaptation of the book was released and earned positive reviews from both critics and audiences. Gundersen, Kathryn. “Many of them even have above-average intelligence, and they tend to be sharp-witted, opinionated kids who just happen to have facial differences.”. Cari tahu serba-serbi kisah Auggie dalam buku novel Wonder, yuk! Raras pero no invisibles. Children born with either Treacher Collins syndrome or other craniofacial conditions have normal intelligence. If you make a purchase using the links included, we may earn commission. Cynthia Murphy was born with the rare craniofacial disorder, Treacher Collins Syndrome - a genetic disorder characterised by the deformity of the eyes, ears, cheekbones and chin, affecting only one in 50,000 people. How prevalent the signs and symptoms of this disorder are can vary greatly. “If it’s causing a problem, whether it’s someone’s eyelids, or their hearing, or skin changes in their cheeks, there is a surgery that can address it,” says Dr. Hopper. Treacher Collins syndrome is a birth defect that affects the head and face. Dr. Hopper has even developed a new procedure that “rotates the entire face” and lengthens bones in the jaw, allowing patients living with a tracheostomy to breathe on their own. Some children born with TCS have problems speaking; if this is the case, the child may be sent to speech therapy from an early age. Im Jahr 2019 folgte die Filmkomödie Good Boys, in der er neben Brady Noon und Keith L. Williams die Hauptrolle spielte. I was alone, in a shared hospital room, at about 4 o’clock in the morning. Filmens hovedperson August lider nemlig af Treacher Collins syndrom, præcis som Kristian Persson. Doctors explain how to tell if you have a head cold or something more serious that requires medical attention, such as the flu, strep throat, meningitis, or mono. Sindrom Treacher Collins adalah kondisi langka. this link is to an external site that may or may not meet accessibility guidelines. Lionsgate. Auggie is a fifth-grade boy with Treacher Collins syndrome who battles the same emotional ups and downs that Dr. Goodman battled. Those affected generally have average intelligence. Treacher Collins syndrome atau TCS juga dikenal dengan nama mandibulofacial dysostosis. Kennedy, Patrick ed. 5. Sindrom Treacher Collins. GradeSaver, 15 January 2016 Web. As I mentioned in a post last month, I’ve decided to branch out beyond telling only our tale and instead feature some of the amazing families I’ve been lucky enough to connect with whose children have Treacher Collins Syndrome (TCS). In 2017, director Stephen Chbosky shone a light on Treacher-Collins Syndrome in his film Wonder. In Wonder (2017), the film adaptation of the 2012 novel of the same name by R. J. Palacio, Roberts played the mother of a boy with Treacher Collins syndrome. Life Expectancy Of Treacher Collins Syndrome. The segment covered the story of Nathaniel Newman, a boy with Treacher Collins Syndrome, who was basically going through the same thing as the character Auggie from Wonder (2017). After being home-schooled for years, he begins school at Beecher Prep. Wonder. They live in New York City. Auggie, anak pengidap Treachers Collin Syndrome dalam film “Wonder” (Sumber: Yahoo) Sindrom Treacher Collins (TCS) adalah kelainan atau cacat lahir bawaan ketika perkembangan tulang dan jaringan di wajah bayi tidak sempurna.. Sindrom Treacher Collins adalah kondisi yang membuat bayi baru lahir mengalami kelainan bentuk telinga, kelopak mata, tulang pipi, dan tulang rahang. Ruthie Lorraine. Is Treacher Collins syndrome contagious? Not affiliated with Harvard College. Treacher Collins syndrome. … Wonder study guide contains a biography of R.J. Palacio, literature essays, quiz questions, major themes, characters, and a full summary and analysis. You can watch the segment from 20/20 by following this link. Richard Hopper, MD, surgical director of Seattle Children’s Craniofacial Center and chief of the division of plastic surgery, treats children with Treacher Collins syndrome, many of whom have also needed multiple operations and highly specialized care. Agrupación de electores DER . why does julian not want a strict teacher. “They wouldn’t want to go hiking out in the woods and suddenly experience a life-threatening breathing problem.”. Explore classroom activities, puzzles, teacher ღೋ ೋღ SUEÑOS MAGICOS ღೋ ೋღ. As shown in the movie, however, growing up with a facial deformity can be tough—and it’s not uncommon for children and adults with Treacher Collins syndrome to feel isolated, frustrated, or depressed. The symptoms of anxiety can be hard to detect. Because he looks different from most kids in middle school, Auggie and his parents are forced to deal with bullying and hurt feelings and to address misconceptions held by teachers and other students. Treacher Collins Syndrome Treatment. After the book came out, she met Magda and Russel Newman, whose son Nathaniel was born with Treacher Collins syndrome, a rare craniofacial disorder that's caused by mutations in a specific gene. - Det er en tilstand, der betyder, at jeg har haft det svært. Wonder is a children’s novel by R.J. Palacio and was published in 2012. “These kids can’t even [travel] easily, because they need to stay near a hospital,” he adds. Each product we feature has been independently selected and reviewed by our editorial team. Treacher Collins syndrome (TCS) is a genetic disorder characterized by deformities of the ears, eyes, cheekbones, and chin. Treacher Collins syndrome (TCS) is a rare, genetic disorder that is characterized by abnormalities in how the face develops. It affects an estimated 1 in 50,000 people in the United States. Sindrom Treacher Collins … People with experience in Treacher Collins syndrome help solve this question. TCS je karakteriziran kongenitalnim simetričnim abnormalnostima lubanje i lica. After being home-schooled for years, he begins school at Beecher Prep. He finds friends in Jack, Charlotte, and Summer, but he must learn to deal with bullying, betrayal, and misunderstandings. In Wonder, Auggie Pullman reveals that he was born with a condition called mandibulofacial dysostosis, which is more commonly known as Treacher Collins Syndrome. In Wonder, Auggie refers to his condition as Mandibulofacial Dysostosis, which is also known as Treacher Collins syndrome (TCS). A similar form of hearing impairment occurs in about 50% of affected individuals. Because it’s so rare, he says (and also so visible), it’s common for people to make assumptions about the disorder without knowing the facts. The story of August “Auggie” Pullman, who was born with a rare facial deformity called Treacher Collins Syndrome and a cleft palate. I might not make the ending as "happy" in the book, only because I am a little more pessimistic about society in general. Once a child is diagnosed, he or she will likely need to be cared for by a team of specialists, including surgeons who specialize in facial deformities and their related health risks. Treacher Collins syndrome is a condition that affects the development of bones and other tissues of the face. Surgery can also address hearing and vision problems. • The facial profile of patients with TCS as fish-like or bird-like. If you were the author of wonder, what would you change in the story? They are involved in making proteins that help make ribosomal RNA (rRNA). When a person is affected by TCS, his/her cheekbones and jawbones do not develop well. Treacher Collins syndrome is a condition that affects the development of bones and other tissues of the face. Treacher Collins syndrome is a craniofacial deformity, meaning that the bones and tissues of the face do not develop as they should. The character, Auggie, was born with Treacher Collins Syndrome, characterized by multiple anomalies such as absent cheekbones and ears, diminutive jaw, near deafness and the need for a tracheostomy. In Wonder, Auggie refers to his condition as Mandibulofacial Dysostosis that is also known as Treacher Collins syndrome (TCS). Mutasi genetik merupakan perubahan kondisi DNA seseorang, teman-teman. The material in this site is intended to be of general informational use and is not intended to constitute medical advice, probable diagnosis, or recommended treatments. For a Haverhill family, the movie "Wonder" headed to the big screen on Friday will be more than a just a movie, it will be an opportunity. Hannah Klein is 12-years-old and like Auggie in the book and movie, Hannah has the genetic condition known as Treacher Collins Syndrome, … From easier cramps to a heavier flow, here's a guide on what to expect decade by decade. Some of the eye abnormalities can lead to vision loss, and unusual ear formation may result in hearing loss. In media interviews, Wonder makeup designer Arjen Tuiten said he relied on prosthetics and heavy makeup to help Tremblay resemble a boy with Treacher Collins syndrome. Treacher Collins is an extremely rare congenital craniofacial disorder caused by mutations in the POLR1C gene. Explore classroom activities, puzzles, teacher The film is helping spread awareness about kids just like their own Wonder Girl. Kondisi ini dikenal dengan nama sindrom Treacher Collins, teman-teman. Treacher Collins syndrome (TCS) is caused by changes (mutations) in any of several genes: TCOF1 (in over 80% of cases), POLR1C, or POLR1D.In a few cases, the genetic cause of the condition is unknown. What are the routes of contagion? Sindrom ini disebabkan oleh mutasi genetik. Treacher Collins — a congenital disorder in which underdeveloped bones in the face and jaw cause sloped eyes, missing or malformed ears and … WBZ-TV's Paula Ebben Kinds of Problems your Child Could Have. Federación Española de Enfermedades Raras. With the movie Wonder coming to theaters this fall, I feel incredibly passionate about trying… In Wonder, Auggie Pullman reveals that he was born with a condition called mandibulofacial dysostosis, which is more commonly known as Treacher Collins Syndrome. Der Der With the movie Wonder coming to theaters this fall, I feel incredibly passionate about trying to highlight the real stories of Wonder. Complications may include breathing problems, problems seeing, cleft palate, and hearing loss. This story is used in a scene from the film, where Jack Will's mother is reminding him … • Treacher–Collins syndrome occurs as an autosomal-dominant disorder in 1 per 50 000 live births, 60% of cases arise as sporadic mutations. “That’s why it’s particularly rewarding to treat these kids with Treacher Collins, because they have so much amazing potential that we can help them reach.”. The Question and Answer section for Wonder is a great This disease is an inherited disorder, and there are very few people affected (about 1 in 70,000 of births in the USA). Mutasi genetik merupakan perubahan kondisi DNA seseorang, teman-teman. ... TREACHER-Collins syndrome affects the bones and face, and is present from birth. What is the main theme of wonder? Wonder is the story of Auggie, a 10-year-old boy who has Treacher Collins Syndrome, a condition that causes numerous physical deformities and impairments. Most affected individuals have underdeveloped facial bones, particularly the cheek bones, and a very small jaw and chin (micrognathia). Sade. Here's What to Do, 9 Signs It's More Serious Than the Common Cold, How Your Period Changes During Your 20s, 30s, and 40s, 12 Anxiety Symptoms That Might Point to a Disorder, Shannen Doherty Reveals Stage 4 Breast Cancer Diagnosis—Here's What It Means, The Best (and Worst) Diets of 2020, According to Experts, 10 Moves for a Cardio Workout at Home—No Equipment Required, These 13 Women Prove Every Body Is a Bikini Body, 20 Things You Should Throw Away for Better Health, 7 Popular TV Shows That Get Mental Health Right. Severity of the … Clean out expired products and clutter to make way for a healthier you. Zackary's Treacher Collins Syndrome … I did not know Landon had Treacher Collins Syndrome before she was born. © Copyright 2021 Meredith Corporation. Only about one in every 50,000 babies born in the United States will have Treacher Collins syndrome. How to handle a physician who doubts or dismisses your symptoms. It gets its name from surgeon Edward Treacher Collins, who first described its traits in 1900. The degree to which a person is affected, however, may vary from mild to severe. It occurs in around 1 out of 10,000 births and therefore, it is considered a rare condition. ICD10-Code: Q75.4 2 Geschichte. “Actually, they tend to be extremely normal children,” says Dr. Hopper. • The orbit is egg shaped; its base is located … "I'm petrified," the actress said when she shared the news that her breast cancer came back. Complications can include an underdeveloped lower jaw that can cause breathing difficulties, eyelids that don’t fully protect the eyes, a cleft palate that affects speech, and hearing problems due to ear abnormalities. FIAPAS. If the parents of the affected child are not affected by the syndrome, the chances of a sibling having Treacher Collins are minimal. Around the same time this movie came out, there was a piece done on ABC’s 20/20 called “Wonder Boy”. Der Spielfilm „Wunder“ erzählt von „Auggie“. Cassie Nicholas who has Treacher Collins Syndrome. About 40% of the time, one parent has Treacher Collins Syndrome. Treacher Collins Syndrome affects the development of bones and other facial tissues. I completely respect the ending in the book, and I can see why the... Jack pretended that he wasn't letting the other students get to him about their treatment of August, as well as the way they treated him over their friendship. Is Treacher Collins syndrome transmitted from person to person? As new movie Wonder is released, 20/20 follows Nathaniel Newman, a boy who has Treacher Collins syndrome but has managed to thrive despite his condition. The new movie “Wonder” showcases the physical and mental ups and downs of a young boy named Auggie who has Treacher Collins syndrome and other facial abnormalities. Unlike Down syndrome, people with Treacher Collins tend to have a life expectancy similar to the population average. Kids with Treacher Collins syndrome may need to have a hole cut into their windpipe with a breathing tube inserted (called a tracheostomy) and may need special hearing aids that transmit sound through bone tissue. Treacher Collins Syndrome is believed to be caused by a change in the gene on chromosome 5, which affects facial development. Wonder. Treacher Collins syndrome is a rare genetic condition that affects the way a child’s face develops, especially the cheekbones, jaws, ears and eyelids. Beim Treacher-Collins Syndrom handelt es sich um eine seltene (1:50.000 Geburten), autosomal-dominant vererbte Krankheit, die mit variabel ausgeprägten Dysmorphien des Gesichtsschädels einhergeht. This is an inherited developmental disorder with a prevalence estimated to range between 1 in 40,000 to 1 in 70,000 of live births. Treacher-Collins Syndrome. Severity of the condition varies from child to child, says Dr. Hopper. Auggie, anak pengidap Treachers Collin Syndrome dalam film “Wonder” (Sumber: Yahoo) Sindrom Treacher Collins (TCS) adalah kelainan atau cacat lahir bawaan ketika perkembangan tulang dan jaringan di wajah bayi tidak sempurna.. Sindrom Treacher Collins adalah kondisi yang membuat bayi baru lahir mengalami kelainan bentuk telinga, kelopak mata, tulang pipi, dan tulang rahang. With no cure for the condition, patients often undergo various surgeries to try and reduce the severity of their facial deformities. Dr. Goodman sees so much of himself in Auggie Pullman, the main character in the newly released movie “Wonder,” based on the book by the same name. This condition is very rare, occurring in only 1 in 50,000 births. Five-year-old Cassie Nicholas has Treacher Collins Syndrome, an extremely rare genetic condition that affects the development of the bones in her face, just like the fictional character in the movie. Im selben Jahr sprach er in einer Folge der Animationsserie Harley Quinn die Figur Damian Wayne alias … Here’s what he wants everyone to know about real-life children—and adults—with a condition like Auggie’s. Here's what you should know about Auggie Pullman's facial disorder before seeing the tearjerker. Auggie's Condition: Treacher Collins Syndrome (TCS). Treacher collins syndrome Franceschetti syndrome or mandibulofacial dysostosis was also known as Treacher Collins syndrome (TCS) is a genetic disorder that causes craniofacial deformities. A July 1977 New York Times article that was reprinted in numerous newspapers nationwide over the ensuing weeks brought this malady to many people's attention for the first time. Treacher Collins Syndrome is a genetic disorder characterized by severe craniofacial malformations. Perhaps the biggest misconception about people with Treacher Collins syndrome is that they’re mentally challenged or not as smart as other people. Red Hot Chili Peppers. All rights reserved. Is Your Doctor Gaslighting You? It gets its name from surgeon Edward Treacher Collins, who first described its traits in 1900. Julia Roberts - Wikipedia In 2017, he starred as August Pullman, a child with Treacher Collins syndrome, in the drama Wonder, and in 2019 he headlined the R-rated comedy film Good Boys. Dysostosis mandibulofacialis) ist eine erbliche Erkrankung, die zu Gesichtsfehlbildungen (craniofaziale Dysmorphie) führt.. Zu den Kennzeichen gehören: Fehlen oder Fehlbildung von Ohren und Jochbein, Gaumenspalte, „fliehendes“ Kinn (Mikrognathie), sowie Augenlidabnormitäten. Children with this condition have very small or partially absent cheek bones and notches in or stretching of the lower eyelids. Aspas Valencia. Das Treacher-Collins-Syndrom oder auch Franceschetti-Syndrom (Dysostosis mandibulofacialis) gehört zu den seltenen Erkrankungen und betrifft eines von 50.000 Neugeborenen. To get our top stories delivered to your inbox, sign up for the Healthy Living newsletter. 1 in 50,000 blog-Treacher Collins Syndrome. Der Junge trägt meist einen Astronautenhelm, um nicht angestarrt zu werden wegen seiner Fehlbildung im Gesicht. But unlike most young men, Jono has Treacher Collins syndrome, a genetic disorder that affected the way his facial bones developed while he was in his mother's womb. (If you're wondering how to pronounce the syndrome, Treacher rhymes with "teacher.") Wyatt Andrews is a four year old boy living with Treacher Collins Syndrom (TCS). (Occasionally, it can be diagnosed during pregnancy via an ultrasound.) Cari tahu serba-serbi kisah Auggie dalam buku novel Wonder, yuk! Treacher Collins syndrome is a genetic disorder that causes defects in the cranium and facial features. The signs and symptoms of this disorder vary greatly, ranging from almost unnoticeable to severe. Offers may be subject to change without notice. “In some children, it’s barely noticeable, and they may need very little care,” he says, “while others can develop very serious complications and need multiple, intensive surgeries.”. Her son cried at the sight of this boy. Treacher Collins is a condition in which the cheek-bones and jawbones are underdeveloped. TCS cannot be cured, but certain treatments may address its symptoms. People with Treacher Collins often have missing cheekbones, downward slanting eyes, hearing loss, atypical or missing ears, and a smaller jaw. Without proper treatment, Treacher Collins syndrome can make it difficult for people to live a normal, healthy life. There is no cure, but surgery can make a big difference. See the fact file below for more information on the Treacher Collins Syndrome or alternatively, you can download our 21-page … Treacher Collins syndrome is usually diagnosed shortly after birth, when it’s clear that a baby’s facial bones and tissues are underdeveloped. In newborns, immediate attention to swallowing and airway problems is critical. The new movie Wonder, based on the bestselling novel of the same name, follows the emotional ups and downs of the Pullman family as they send their 10-year-old son August off to fifth grade. Treacher Collins syndrome is a genetic condition. Sindrom ini disebabkan oleh mutasi genetik. In media interviews, Wonder makeup designer Arjen Tuiten said he relied on prosthetics and heavy makeup to help Tremblay resemble a boy with Treacher Collins syndrome. The signs and symptoms of this disorder vary greatly, ranging from almost unnoticeable to severe. Simptomi. R.J. Palacio got the inspiration to write the book after taking her son out for ice cream, where they saw a child with Treacher Collins Syndrome. Die Krankheit, unter der Auggie im Buch und im Film Wunder leidet, nennt sich Treacher-Collins-Syndrom. Wonder is about a boy with a severe facial deformity disorder called Treacher Collins Syndrome and he is sent to a local public school after being home schooled by his mother for the first several years of his life. • The facial profile of patients with TCS as fish-like or bird-like. Underdeveloped facial bones may restrict an infant's airway, resulting in respiratory problems. Hearing loss is also associated with this syndrome. Das Treacher-Collins-Syndrom (Synonyme: Franceschetti-Zwahlen-Syndrom, Berry-Syndrom bzw. Nirvana. resource to ask questions, find answers, and discuss the novel. 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