Childhood Disintegrative Disorder Overview

Childhood Disintegrative Disorder Overview
Childhood disintegrative disorder is a severe loss of social, communication and other skills classified in a group of disorders called “Pervasive Developmental Disorders.” Onset is usually after the age of four. The signs and symptoms are similar to autism, although autism usually occurs at an earlier age and is more common.
Pervasive developmental disorders include:
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Childhood disintegrative disorder
Autism
Asperger’s syndrome
Rett syndrome
Pervasive developmental disorder not otherwise specified
A Viennese educator, Theodor Heller, first described the condition. Childhood disintegrative disorder is also known as Heller’s syndrome after Theodor Heller.
Signs and symptoms of childhood disintegrative disorder include:
Normal development for at least the first two years of life
Significant loss of previously acquired or learned skills before age 10 in at least two of the following areas:
1. ability to say words or sentences
2. ability to understand verbal and nonverbal communication
3. social skills and self-care skills
4. bowel and bladder control
5. play skills
6. motor skills (ability to voluntarily move the body in a purposeful way)
The lack of impairment occurs in at least two of the following areas:
1. social interaction
2. communication
3. repetitive and stereotyped patterns of behavior, interests and activities
Childhood disintegrative disorder may occur abruptly over the course of days to weeks or gradually over an extended period of time. There is seldom found an underlying medical or neurological cause.
Further research is difficult due to the limited number of children diagnosed with childhood disintegrative disorder, although more research is needed at this time. Experts suspect there may be a genetic basis or that an autoimmune response plays a role in the development of childhood disintegrative disorder.
Treatment
Treatment for childhood disintegrative disorder is about the same as for autism; there is no cure for this disorder. Treatment may include:
Medications: There are no medications specifically to treat childhood disintegrative disorder. Severe behavior problems like aggression and repetitive movements can sometimes be controlled by antipsychotic medications.
Behavior therapy may be used by psychologists, speech therapists, physical therapists and occupational therapists, parents, teachers and caregivers.
Prognosis for children with childhood disintegrative disorder is usually poor and worse than for children with autism. Children with this disorder often need residential care in a group home or long term care facility.
Source: Mayo Clinic
Disclaimer: This article is for educational purposes only. It is not intended to be a substitute for informed medical advice or care. You should not use the information in this article to diagnose or treat any health problems or illnesses without consulting your pediatrician or family doctor. Please consult a doctor with any questions or concerns you might have regarding your or your child’s condition.
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Watch the video related to Rett Syndrome
Rett syndrome (symbolized RTT) is caused by sporadic mutations in the gene MECP2 located on the X chromosome. It almost exclusively affects girls — male fetuses with the disorder rarely survive to term. Development is typically normal until 6-18 months, when language and motor milestones regress, purposeful hand use is lost and acquired deceleration in the rate of head growth (resulting in microcephaly in some) is seen. Hand stereotypies are typical and breathing irregularities such as …
Help answer the question about Rett Syndrome
what is the best theraphy for rett syndrome?my daughter is 19 years old and she has rett syndrome since 1 year 6 months we go to a lot of doctors but still the same i want to help her even a theraphy for my own because the doctors said its her fate to be like that . She is like a baby to take care
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Hello…my 3 1/2 year old daughter has Rett Syndrome. Luckily she doesn't have scoliosis yet. From other parents I have talked to, surgery for scoliosis is somewhat common but I think its mostly done when it is affecting their ability to breathe. The other 2 surgeries I have never heard of being done on girls with RS. My daughter has problems with her ankles that we brace. If there is tightening I have heard of parents trying botox with good results. But sleep apnea is pretty common in RS I think also…yet I have never heard of tonsils being taken out. You have to be VERY careful with surgeries because girls with RS have difficulties with pneunomia, the anesthesia, recovery, and seizures tend to increase with the pain from it. Are you on the Rettnet? If not, that is your best source of answers because it is a huge community of parents, therapists, Drs, etc. That is who you should be asking those questions. You can sign up for it at http://www.rettsyndrome.org. Best of luck to you and your sister!
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