Tourette Syndrome Hotline

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Tourette Syndrome and Other Tic Disorders. The prevalence of TS varies based on study design and location. An international prevalence of 0.6% – 1% has been reported for mainstream schoolchildren, with the disorder being 3–4 times more common in males than in females (Cavanna and Termine 2012).Data from the 2007 National Survey of Children's Health (NSCH) …

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Underlying Risk Factors and Metabolic Syndrome. The predominant underlying risk factors for the syndrome appear to be abdominal obesity 2–4 and insulin resistance 5,6; other associated conditions can be physical inactivity, 3,7 aging, 8 and hormonal imbalance. 9 An atherogenic diet (eg, a diet rich in saturated fat and cholesterol) can enhance risk for …

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A number of other disorders often occur along with tic symptoms. For example, more than 50% of people with Tourette's syndrome also have attention-deficit hyperactivity disorder, and approximately 30% to 40% also have obsessive-compulsive disorder.

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THE MIAMI HERALD: Is Cuba responsible for 'Havana syndrome'? Secretary of State Antony Blinken announced Friday he’s appointing two veteran diplomats to lead the State Department’s efforts on

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Contact Lens Overwear Syndrome (also known as contact lens-induced acute red eye, CLARE, or tight lens syndrome) is the result of patients over-extending their contact lens wearing time or by wearing their contact lenses in a closed eye environment

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Please note that these questions are not monitored 24/7. You can expect a response within about one week of submitting. *If you are a patient of the Adult Down Syndrome Center and have a question about your care, please call the Center

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847-318-2377

Adult Down Syndrome Center. 1610 Luther Lane. Park Ridge, IL 60068. Phone 847-318-2303. Fax 847-318-2377. facebook youtube playlist. Join our mailing list: Sign up to receive emails with information on health topics for teens and adults

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Battered woman syndrome is caused by domestic abuse. While it’s something that can happen between intimate partners, the term “domestic abuse” is an umbrella term that can include things

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Battered Woman Syndrome, also known as Battered Person Syndrome, is a collection of signs and symptoms that sadly occur with such regularity in people who are persistently battered, so as to be predictable. The battering can be physical, emotional,

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Settanni CR, Ianiro G, Ponziani FR, Bibbò S, Segal JP, Cammarota G, Gasbarrini A. COVID-19 as a trigger of irritable bowel syndrome: A review of potential mechanisms. World J Gastroenterol 2021; 27 (43): 7433-7445 [DOI: 10.3748/wjg.v27.i43.7433] Cor

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The Neuroleptic Malignant Syndrome Information Service was founded in 1997 by the Malignant Hyperthermia Association of the United States (MHAUS) to advance awareness of neuroleptic malignant syndrome. This is a life-threatening neurological disorde

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Yet nails can also turn color due to stains from tobacco, henna or self-tanning products. A non-cosmetic cause can be yellow nail syndrome . Yellow nail syndrome nails appear thick and yellow/green in which case it’s time for a visit to the doctor’s office.

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Chronic Fatigue Syndrome Disability Benefits Questionnaire Updated on: April 2, 2020~v20_1 . Released March 2021 Page 1. CHRONIC FATIGUE SYNDROME (CFS) DISABILITY BENEFITS QUESTIONNAIRE. NAME OF PATIENT/VETERAN. PATIENT/VETERAN'S SOCIAL SECURITY NUMBER Note - The Veteran is applying to the U.S. Department of Veterans Affairs

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Parsonage-Turner syndrome (PTS) is an uncommon neurological disorder characterized by rapid onset of severe pain in the shoulder and arm. This acute phase may last for a few hours to a few weeks and is followed by wasting and weakness of the muscles (amyotrophy) in the affected areas.

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Silver-Russell Syndrome (SRS) is typically characterized by asymmetric gestational growth restriction resulting in affected individuals being born small for gestational age, with relative macrocephaly at birth (head circumference ≥1.5 SD above birth weight and/or length), prominent forehead usually with frontal bossing, and frequently body asymmetry.

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General Discussion. Cat eye syndrome (CES) is a rare chromosomal disorder that may be evident at birth. Individuals with a normal chromosomal make-up have two 22nd chromosomes, both of which have a short arm, known as 22p, and a long arm, known as 22q.

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In Alport syndrome (AS) a spectrum of phenotypes ranging from progressive renal disease with extrarenal abnormalities to isolated hematuria with a non-progressive or very slowly progressive course is observed. Approximately two thirds of AS is X-linked (XLAS); approximately 15% is autosomal recessive (ARAS), and approximately 20% is autosomal dominant (ADAS).

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The drug helps treat patients with Lennox-Gastaut syndrome and Dravet syndrome, two types of debilitating epilepsy. On this list of medicinal marijuana stories, you’ll find out how medical cannabis changed the lives of people who thought they had no hope left. 1. Rebecca Sewell

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Introduction. The Metabolic Syndrome (MetS) has been called a global epidemic by the WHO 1 and is considered a major public health problem, 2 with 34% of Americans over the age of 20 estimated to be affected. 3–4 Among adolescents, 9.4% are estimated to have MetS and the prevalence rises to 44.2% among those that are obese. 5 Therefore, the MetS is one of the few …

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Werner syndrome is a rare disorder that affects males and females in equal numbers. Since the disorder was originally described in the medical literature in 1904 (O. Werner), more than 800 cases have been reported.

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Stiff person syndrome (SPS) is a progressive syndrome characterized by recurrent episodes of severe muscle stiffness, rigidity, and painful spasms in the trunk and limbs. The age that symptoms begin can vary, but most people start experiencing symptoms between ages 30 and 60. Spasms can be prolonged and extremely forceful, with the ability to generate enough …

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Investigating Savant Syndrome . Savant syndrome is interesting to the public, but no one knows the exact number of people who have this syndrome. Some studies suggest that as many as one in 10 people with autism have some degree of savant syndrome.

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A very small number of newborns survive following intrauterine transfusions and repeated frequent transfusions after birth. ... [Steensma et al 2005]. Red cell indices are usually hypochromic and microcytic, in contrast to the normocytic or macrocytic indices typical of myelodysplastic syndrome. ... Phone: +357 22 319129. Fax: +357 22 314552.

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Long QT syndrome (LQTS) is a cardiac electrophysiologic disorder, characterized by QT prolongation and T-wave abnormalities on the EKG that are associated with tachyarrhythmias, typically the ventricular tachycardia torsade de pointes (TdP). TdP is usually self-terminating, thus causing a syncopal event, the most common symptom in individuals with …

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Kabuki syndrome (KS) is characterized by typical facial features (long palpebral fissures with eversion of the lateral third of the lower eyelid; arched and broad eyebrows; short columella with depressed nasal tip; large, prominent, or cupped ears), minor skeletal anomalies, persistence of fetal fingertip pads, mild-to-moderate intellectual disability, and postnatal …

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Metformin is a biguanide used since the 1960’s in the treatment of type 2 diabetes and metabolic syndrome. It enhances insulin sensitivity, induces glycolysis and suppresses gluconeogenesis in the liver 1–3.Patients with metabolic syndrome exhibit many manifestations of accelerated aging, such as cardiovascular disease, cancer and inflammatory disorders, all of which reduce lifespan.

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Stickler syndrome affects males as well as females. Prevalence rates have been estimated at 1-3 per 10,000 births and at 1 per 7,500 births. Most investigators believe that the disorder is highly under-diagnosed, making it difficult to determine the true prevalence of Stickler syndrome in the general population.

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Peeling skin syndrome belongs to the groups of congenital ichthyosis and skin fragility disorders with autosomal recessive inheritance. Most forms of PSS manifest at birth or during infancy with shedding or peeling of the outermost layer of the skin (horny layer, aka stratum corneum).

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According to a national health survey, more than 1 in 5 Americans has metabolic syndrome. The number of people with metabolic syndrome increases with age, affecting more than 40% of people in their 60s and 70s. Who typically has metabolic syndrome? People with central obesity (increased fat in the abdomen/waist).

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Pfeiffer syndrome is now known to be a member of a group of conditions caused by mutations in the FGFR genes including Apert syndrome, Crouzon syndrome, Beare-Stevenson syndrome, FGFR2-related isolated coronal synostosis, Jackson-Weiss syndrome, Crouzon syndrome with acanthosis nigricans and Muenke syndrome. (For more information on these ...

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Cushing syndrome is the clinical manifestation of pathological hypercortisolism from any cause. Patients often display weight gain with central obesity, facial rounding and plethora, proximal muscle weakness, and thinning of the skin.

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Kearns-Sayre syndrome is caused by defects in mitochondria, which are structures within cells that us oxygen to convert the energy from food into a form that can be used by cells. This process is called oxidative phosphorylation.Although most DNA is packaged in chromosomes within the nucleus (nuclear DNA), mitochondria also have a small amount of …

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March 26, 2018 Embassy of Iceland in London Facts about Down's syndrome and pre-natal screening in Iceland

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Maternal 15q duplication syndrome (maternal dup15q) is characterized by hypotonia and motor delays, intellectual disability, autism spectrum disorder (ASD), and epilepsy including infantile spasms. Rarely, maternal dup15q may also be associated with psychosis or sudden unexplained death. Those with a maternal isodicentric 15q11.2-q13.1 supernumerary …

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Kline AD, Grados M, Sponseller P, et al. Natural history of aging in Cornelia de Lange syndrome. Am J Med Genet C Semin Med Genet. 2007;Aug 15;145C(3):248-60. Kline AD, Krantz ID, Sommer A, et al. Cornelia de Lange syndrome: clinical review, diagnostic and scoring systems, and anticipatory guidance. Am J Med Genet. 2007;143A:1287-1296.

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Puberty Syndrome—a rumored, mysterious syndrome that only affects those in their puberty. For example, a bunny girl suddenly appeared in front of Sakuta Azusagawa. The bunny girl's real identity is Mai Sakurajima, a teenage celebrity who is currently an inactive high school senior. For some reason, her charming figure does not reflect in the eyes of others.

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TDO syndrome is one of a group of congenital disorders known as ectodermal dysplasias. The condition primarily affects hair which is strikingly curly, and the teeth. X-ray examination of persons with TDO syndrome usually shows a mild increase in bone density, particularly in …

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Cho WK, Park JW, Park MR. Surgical correction of Hallermann-Streiff syndrome: a case report of esotropia, entropion, and blepharoptosis. Korean J Ophthalmol. 2011;25:142-145.

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Stockholm Syndrome knows no bounds, it can be found in all kinds of interpersonal relationships in the context of social, cultural and other influences; For example, families, intimate relationships, friendships, marriage, parent-child, the workplace, social …

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Most characteristically, Aicardi-Goutières syndrome (AGS) manifests as an early-onset encephalopathy that usually, but not always, results in severe intellectual and physical disability. A subgroup of infants with AGS present at birth with abnormal neurologic findings, hepatosplenomegaly, elevated liver enzymes, and thrombocytopenia, a picture highly …

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Symptoms of the following disorders may be similar to those of Apert syndrome. Comparisons may be useful for a differential diagnosis. Carpenter syndrome is a rare genetic disorder associated with craniosynostosis, webbing or fusion (syndactyly) of certain fingers or toes, and/or extra fingers or toes (polydactyly).

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General Discussion. Summary. Crouzon syndrome is a rare genetic disorder. It is a form of craniosynostosis, a condition in which there is premature fusion of the fibrous joints (sutures) between certain bones of the skull.

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Introduction. Polycystic ovary syndrome (PCOS) is a common endocrine disorder in females, especially in women of reproductive age. The worldwide prevalence of PCOS is estimated to be 5–10%.1 PCOS could be diagnosed by infertility, acne, amenorrhea or oligomenorrhea, hirsutism, insulin resistance, obesity, hyperandrogenism, and polycystic …

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Paediatric Inflammatory Multisystem Syndrome (PIMS) is a new condition that happens weeks after someone has had the virus that causes coronavirus (COVID-19). It causes inflammation (swelling) throughout the body which is one way your immune system fights

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Tourette syndrome, or TS, is an inherited neurological disorder that causes people to make involuntary and uncontrollable vocal sounds and movements, called ‘tics’. Tourette syndrome usually begins between 2 and 21 years of age.

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1800 022 222

Read more about Tourette syndrome. Turner syndrome. This genetic disorder involves sensory, developmental and hormonal symptoms, but most girls and women with Turner syndrome enjoy a normal life. ... Healthdirect 24hr 7 days a week hotline. 24 hour health advice you can count on. 1800 022 222. Government Accredited with over 140 information ...

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1300 659 467

Tourette Syndrome Diagnosis and Treatment, Treatment of TS-related OCD and ADHD. DEPRESSION TEST. ... Lifeline: 13 11 14 (24 hour crisis hotline) Kids Helpline: 1800 55 1800 Online counselling available Mensline: 1300 78 99 78 Suicide Call Back Service: 1300 659 467. Vita Links. Our Services I am a Doctor

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Clonidine is a centrally acting alpha-agonist hypotensive agent, generally used to treat high blood pressure.1 Clonidine has several off-label uses including the management of hypertensive crises, menopausal flushing (hot flashes), Tourette’s syndrome, attention deficit hyperactivity disorder (ADHD), opioid and alcohol withdrawal, smoking cessation, and migraine …

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A special plan for children with Autism, Tourette’s Syndrome or ADHD and their parent Coverage up to RM100,000 death benefit for both child and parent

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Tourette’s Syndrome. Tourette’s Association A nonprofit advocacy organization for individuals and families affected by Tourette’s and other tic disorders and includes: relevant science, treatment options, and a search function to find helping professionals by state. ... This Minnesota suicide hotline is a direct link to counselors.

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  • Frequently Asked Questions

  • What is the Pennsylvania Tourette Syndrome Alliance?

    The Pennsylvania Tourette Syndrome Alliance is a non-profit organization that promotes awareness and acceptance, provides education, and assists families, schools and communities while advocating for individuals with TS. Search Login Donate Now Join Us Home PATSA Mission & History

  • Is Tourette syndrome undiagnosed?

    As many as 1 in 100 individuals show signs of Tourette Syndrome – and most of them undiagnosed, misdiagnosed and/or misunderstood.

  • What is the prevalence of Tourette syndrome in the US?

    37% have been reported as having moderate or severe forms of the condition. Boys are three to five times more likely to have TS than girls. People from all racial and ethnic groups can have TS. Non-Hispanic white children are twice as likely to have a TS diagnosis as Hispanic and non-Hispanic black children.

  • What does socal chapter do for tourette syndrome?

    SoCal Chapter. The Tourette Association of America Southern California Chapter is committed to bringing our community together through education, advocacy, and the creation and sponsorship of social events that are made available to families, children of different age groups, and adults living with Tourette Syndrome. Newly diagnosed?

  • What are tics in Tourette syndrome?

    Tourette Syndrome (TS) is a condition of the nervous system. TS causes people to have “tics”. Tics are sudden twitches, movements, or sounds that people do repeatedly. People who have tics cannot stop their body from doing these things. For example, a person might keep blinking over and over. Or, a person might make a grunting sound unwillingly.

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