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Cotard`s Syndrome
Cotard`s Syndrome

... reported as a special form of Cotard’s syndrome. However, the classification of these delusions as nihilistic delusions concerning one’s body can be debated. A classical description of the course of Cotard’s syndrome is given by Enoch and Trethowan. In its early stages, Cotard’s syndrome is characte ...
cerebellar hemisphere
cerebellar hemisphere

... Department of Neurology ...
Autism - mrsashleymhelmsclass
Autism - mrsashleymhelmsclass

... • Noticeable in babies at about 18 months • Has problems socializing, ...
Sula Wolff - Rebound Therapy
Sula Wolff - Rebound Therapy

... or restricted, repetitive, and stereotyped behaviours. An exclusion criterion is schizotypal disorder, but the definition includes schizoid disorder of childhood and autistic psychopathy. DSM-IV criteria also exclude significant delay of language and cognitive development; indicate that the disturba ...
Bijlage 1 - Steungroep ME en Arbeidsongeschiktheid
Bijlage 1 - Steungroep ME en Arbeidsongeschiktheid

... 34. Ramsay AM. Myalgic encephalomyelitis and postviral fatigue states. 2nd ed. London: Gower Medical Publishing, 1988. ...
Research in Developmental Disabilities Eliciting Neurodevelopmental Clinical Examinations
Research in Developmental Disabilities Eliciting Neurodevelopmental Clinical Examinations

... disability or ADHD. Other groups (e.g. Chawarska, Klin, Paul, Macari, & Volkmar, 2009) have found similar results. In a new study of more than 300 preschool children with a clinical diagnosis of ASD, the vast majority met research DSM-IV criteria for autistic disorder, Asperger’s disorder, or pervas ...
DSM-5: The New Diagnostic Criteria For Autism Spectrum Disorders
DSM-5: The New Diagnostic Criteria For Autism Spectrum Disorders

... A. Persistent difficulties in the social use of verbal and nonverbal communication as manifest by deficits in the following: 1) Using communication for social purposes, such as greeting and sharing information, in a manner that is appropriate for the social context; 2) Changing communication to matc ...
Tourette*s syndrome
Tourette*s syndrome

... years of age. • have symptoms that are not due to taking medicine or other drugs or due to having another medical condition (for example, seizures, Huntington disease, or postviral encephalitis). ...
A Concise History of Asperger Syndrome: The Short
A Concise History of Asperger Syndrome: The Short

... DSM-IV broadened the diagnostic boundaries of Autism, conceived for the first time as a spectrum of disorders that included Autistic Disorder, AS and Pervasive Developmental Disorder Not Otherwise Specified (American Psychiatric Association [APA], 1994). Also new was the inclusion of Childhood Disin ...
Neuro Oncology: Neuroradiology
Neuro Oncology: Neuroradiology

... Syndrome demonstrating moderate atrophy of the brain stem and middle cerebellar peduncle with mild atrophy of the cerebellum, as well as atrophy of the infraorbital and intracranial optic nerves3. ...
Last Review Status/Date
Last Review Status/Date

... joints, hand calluses, velvet-like skin, flat feet and mitral valve prolapse. The characteristic appearance of adult males includes macroorchidism. Patients may show behavioral problems including autism spectrum disorders, sleeping problems, social anxiety, poor eye contact, mood disorders and handf ...
Primary Complex Motor Stereotypies in Older Children and Adolescents: Clinical Features and Longitudinal Follow-Up
Primary Complex Motor Stereotypies in Older Children and Adolescents: Clinical Features and Longitudinal Follow-Up

... abstract BACKGROUND: Complex motor stereotypies are rhythmic, repetitive, fixed, and purposeless movements that stop with distraction. Once believed to occur only in children with autism spectrum or other developmental disorders, their presence in otherwise typically developing children (primary) has ...
MDA INFORMATION FACTSHEET – Mitochondrial
MDA INFORMATION FACTSHEET – Mitochondrial

... abnormalities, seizures, and severe headaches resembling migraines. Repeated stroke-like episodes can progressively damage the brain, leading to vision loss, problems with movement, and a loss of intellectual function (e.g. dementia). If there is a history of developmental delays, learning disabilit ...
MRI of acute stroke.A.
MRI of acute stroke.A.

... Ischemia within the genu of the internal capsule causes primarily facial weakness followed by arm then leg weakness as the ischemia moves posterior within the capsule. Alternatively, the contralateral hand may become ataxic and dysarthria will be prominent (clumsy hand, dysarthria lacunar syndrome). ...
Tourette Syndrome - Canadian Psychological Association
Tourette Syndrome - Canadian Psychological Association

... TS rarely occurs in isolation. Other neurodevelopmental conditions which commonly co-occur with TS are Attention-Deficit/Hyperactivity Disorder (ADHD), Obsessive-Compulsive Disorder (OCD), Learning Disorders, and sensory processing dysfunctions. When an individual must contend with many or all of th ...
What is serotonin syndrome and which medicines cause it?
What is serotonin syndrome and which medicines cause it?

... which usually occurs within a few hours of drug or dose changes, resolving within about 24 hours of stopping the serotonergic drug(s) (5). Symptoms Serotonin syndrome or toxicity results in certain symptoms consisting of a triad of features: alteration of mental status, neuromuscular abnormalities a ...


... signs usually present together with other manifestations such as ataxia, myoclonus, and tremor. Thus, the possibility of ocular tics was entertained. Tics possess three features that can help differentiate them from other movement disorders27: (1) they are often preceded by a sensation and an irresi ...
Treatment in Psychiatry
Treatment in Psychiatry

... increase awareness of autism. He also advocated an approach to education that involved individualized attention, an emphasis on strengths rather than weaknesses, and engagement in learning by tapping into the child’s special interests. These approaches continue to be used today in the education of c ...
Asperger`s Syndrome: Diagnosis and Treatment
Asperger`s Syndrome: Diagnosis and Treatment

... increase awareness of autism. He also advocated an approach to education that involved individualized attention, an emphasis on strengths rather than weaknesses, and engagement in learning by tapping into the child’s special interests. These approaches continue to be used today in the education of c ...
Efficient Practices for Treating the Developmental Disabled
Efficient Practices for Treating the Developmental Disabled

...  May be appropriate to train  May be able to acquire good adaptive skills  Diagnosis required bf age 18 months  Etiology and associations with syndromes may help for early detection (i.e. Down Syndrome)  Mild MR of unknown origin is recognized later More severe MR resulting from acquired cause ...
The Vineland ABS and The Vineland II
The Vineland ABS and The Vineland II

... As a measure to support the diagnosis of other disabilities – Death Penalty Cases and ...
Restless Legs Syndrome in an Elderly Patient Induced by Combined
Restless Legs Syndrome in an Elderly Patient Induced by Combined

... Since the necessary equipment for a polysomniographic evaluation was not present in our hospital, the patient was referred to an outpatient clinic with a polysomniography laboratory. Due to objection of patient, polysomniography could not be done, but the described case fulfills the RLS diagnostic ...
ADHD and Tics or Tourette Syndrome
ADHD and Tics or Tourette Syndrome

... In many cases when a child has both ADHD and tics, the health care professional may elect to treat the ADHD first because primary treatment of ADHD may reduce stress, improve attention and sometimes reduce tics by enhancing the individual’s ability to suppress tics. Treatment options for ADHD includ ...
psychiatric disorders associated with cushing`s syndrome
psychiatric disorders associated with cushing`s syndrome

... Background: Cushing's syndrome is the term used to describe a set of symptoms associated with hypercortisolism, which in most cases is caused by hypophysial microadenoma over-secreting adrenocorticotropic hormone. This endocrine disorder is often associated with psychiatric comorbidities. The most i ...
Catatonia-Webinar 2014
Catatonia-Webinar 2014

... Neurological disorder that manifests itself within the first three years of life (Pervasive Developmental Disorder) Considered a “spectrum disorder” because symptoms and severity vary from person to person Significantly impairs a person’s abilities particularly in the areas of language, communicatio ...
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Rett syndrome

Rett syndrome (RTT), originally termed cerebroatrophic hyperammonemia, is a rare genetic postnatal neurological disorder of the grey matter of the brain that almost exclusively affects females but has also been found in male patients. The clinical features include small hands and feet and a deceleration of the rate of head growth (including microcephaly in some). Repetitive stereotyped hand movements, such as wringing and/or repeatedly putting hands into the mouth, are also noted. People with Rett syndrome are prone to gastrointestinal disorders and up to 80% have seizures. They typically have no verbal skills, and about 50% of affected individuals do not walk. Scoliosis, growth failure, and constipation are very common and can be problematic.The signs of this disorder are most easily confused with those of Angelman syndrome, cerebral palsy and autism. Rett syndrome occurs in approximately 1:10,000 live female births in all geographies, and across all races and ethnicities.Rett syndrome was formerly classified as a pervasive developmental disorder by the Diagnostic and Statistical Manual of Mental Disorders (DSM), together with the autism spectrum disorders and childhood disintegrative disorder. Some argued against this classification because RTT is similar to non-autistic spectrum disorders such as fragile X syndrome, tuberous sclerosis, or Down syndrome where one can see autistic features. It was removed from the DSM-5 in 2013 because it has a known molecular etiology.It was first described by Austrian pediatrician Andreas Rett in 1966. Huda Zoghbi demonstrated in 1999 that Rett syndrome is caused by mutations in the gene MECP2.
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