Autism other diagnostic studies: Difference between revisions

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{{Autism}}
{{Autism}}
{{CMG}}; {{AE}}  
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==Overview==
==Overview==
There are no other diagnostic studies associated with [disease name].
Other diagnostic studies for autism include electroencephalography, metabolic testing, polysomnography and genetic testing to rule out other conditions.
 
OR
 
[Diagnostic study] may be helpful in the diagnosis of [disease name]. Findings suggestive of/diagnostic of [disease name] include [finding 1], [finding 2], and [finding 3].
 
OR
 
Other diagnostic studies for [disease name] include [diagnostic study 1], which demonstrates [finding 1], [finding 2], and [finding 3], and [diagnostic study 2], which demonstrates [finding 1], [finding 2], and [finding 3].


==Other Diagnostic Studies==
==Other Diagnostic Studies==
*Tests to evaluate metabolic disorders:<ref name="pmid18079313">{{cite journal |vauthors=Manzi B, Loizzo AL, Giana G, Curatolo P |title=Autism and metabolic diseases |journal=J. Child Neurol. |volume=23 |issue=3 |pages=307–14 |date=March 2008 |pmid=18079313 |doi=10.1177/0883073807308698 |url=}}</ref>
*Tests to evaluate [[Metabolic disorder|metabolic disorders]]:<ref name="pmid18079313">{{cite journal |vauthors=Manzi B, Loizzo AL, Giana G, Curatolo P |title=Autism and metabolic diseases |journal=J. Child Neurol. |volume=23 |issue=3 |pages=307–14 |date=March 2008 |pmid=18079313 |doi=10.1177/0883073807308698 |url=}}</ref>
**Various metabolic abnormalities include abnormalities involving nucleotides, amino acids, vitamins, and mitochondria may be found in association with autism spectrum disorder. However, screening and testing to investigate metabolic abnormalities are not routinely recommended for the diagnosis of autism spectrum disorder. Unless the patient present with symptoms including seizures, sluggishness, recurrent vomiting, dysmorphic feautures and gross motor and mental retardation.
**Various [[Metabolic disorder|metabolic disorders]]  involving [[Nucleotide|nucleotides]], [[Amino acid|amino acids]], [[Vitamin|vitamins]], and [[Mitochondrial disease|mitochondria]] may be found in association with [[autism spectrum disorder]].
 
**However, screening and testing to investigate [[Metabolic disorder|metabolic abnormalities]], are not routinely recommended for the [[diagnosis]] of [[autism spectrum disorder]]. Unless the patient present with symptoms including [[Seizure|seizures]], [[Lethargy|sluggishness]], recurrent [[Nausea and vomiting|vomiting]], [[Dysmorphic feature|dysmorphic feautures]] and [[Gross motor skill|gross motor]] and [[mental retardation]].
*[[Electroencephalography]]:<ref name="pmid10953176">{{cite journal |vauthors=Filipek PA, Accardo PJ, Ashwal S, Baranek GT, Cook EH, Dawson G, Gordon B, Gravel JS, Johnson CP, Kallen RJ, Levy SE, Minshew NJ, Ozonoff S, Prizant BM, Rapin I, Rogers SJ, Stone WL, Teplin SW, Tuchman RF, Volkmar FR |title=Practice parameter: screening and diagnosis of autism: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Child Neurology Society |journal=Neurology |volume=55 |issue=4 |pages=468–79 |date=August 2000 |pmid=10953176 |doi= |url=}}</ref>
**[[Electroencephalography]] is not routinely indicated to diagnose autism spectrum disorder.
** May be indicated in certain conditions, to evaluate [[autism spectrum disorder]] presenting with [[Seizure|seizures]], landau-kleffner syndrome ([[aphasia]] with seizures).
*[[Polysomnography]]:<ref name="pmid17252887">{{cite journal |vauthors=Malow BA, Marzec ML, McGrew SG, Wang L, Henderson LM, Stone WL |title=Characterizing sleep in children with autism spectrum disorders: a multidimensional approach |journal=Sleep |volume=29 |issue=12 |pages=1563–71 |date=December 2006 |pmid=17252887 |doi= |url=}}</ref>
**Abnormalities in [[sleep]] pattern such as frequent wakeups, early morning arousals, and altered sleep  are commonly found in children with [[Autism spectrum disorder|autism spectrum disorder.]]
**[[Polysomnography]] may be helpful in evaluation of these conditions.
*Genetic testing:
**As per recommendations of the American academy of neurology and the child neurology society, genetic testing is indicated in cases of autism and fragile X syndrome.


==References==
==References==
{{Reflist|2}}
{{Reflist|2}}


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Latest revision as of 15:55, 2 April 2018

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Chandrakala Yannam, MD [2]

Overview

Other diagnostic studies for autism include electroencephalography, metabolic testing, polysomnography and genetic testing to rule out other conditions.

Other Diagnostic Studies

References

  1. Manzi B, Loizzo AL, Giana G, Curatolo P (March 2008). "Autism and metabolic diseases". J. Child Neurol. 23 (3): 307–14. doi:10.1177/0883073807308698. PMID 18079313.
  2. Filipek PA, Accardo PJ, Ashwal S, Baranek GT, Cook EH, Dawson G, Gordon B, Gravel JS, Johnson CP, Kallen RJ, Levy SE, Minshew NJ, Ozonoff S, Prizant BM, Rapin I, Rogers SJ, Stone WL, Teplin SW, Tuchman RF, Volkmar FR (August 2000). "Practice parameter: screening and diagnosis of autism: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Child Neurology Society". Neurology. 55 (4): 468–79. PMID 10953176.
  3. Malow BA, Marzec ML, McGrew SG, Wang L, Henderson LM, Stone WL (December 2006). "Characterizing sleep in children with autism spectrum disorders: a multidimensional approach". Sleep. 29 (12): 1563–71. PMID 17252887.

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