Autistic disorder in 2 children with mitochondrial disorders

被引：33

作者：

Tsao, Chang-Yong ^{[1
]}

Mendell, Jerry R. ^{[1
]}

机构：

[1] Ohio State Univ, Dept Pediat & Neurol, Columbus, OH 43210 USA

来源：

JOURNAL OF CHILD NEUROLOGY | 2007年 / 22卷 / 09期

关键词：

mitochondrial; autism;

D O I：

10.1177/0883073807306266

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

Autistic disorder is a heterogeneous disorder. The majority of the cases are idiopathic, and only a small number of the autistic children have associated secondary diagnosis. This article reports 2 children with mitochondrial disorders associated with autistic disorder fulfilling the diagnostic criteria of the American Psychiatric Association Manual of Psychiatric Diseases, 4th edition, and briefly reviews the literature on autistic disorder associated with mitochondrial disorders.

引用

页码：1121 / 1123

页数：3

共 21 条

[1]

BARKOVICH AJ, 1993, AM J NEURORADIOL, V14, P1119

[2] Brain MRI and proton MRS findings in infants and children with respiratory chain defects [J].

Dinopoulos, A ;

Cecil, KM ;

Schapiro, MB ;

Papadimitriou, A ;

Hadjigeorgiou, GM ;

Wong, B ;

deGrauw, T ;

Egelhoff, JC .

NEUROPEDIATRICS, 2005, 36 (05) :290-301

[3] Mitochondrial dysfunction in patients with hypotonia, epilepsy, autism, and developmental delay:: HEADD syndrome [J].

Filiano, JJ ;

Goldenthal, MJ ;

Rhodes, CH ;

Marín-García, J .

JOURNAL OF CHILD NEUROLOGY, 2002, 17 (06) :435-439

[4] Practice parameter: Screening and diagnosis of autism - Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Child Neurology Society [J].

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 .

NEUROLOGY, 2000, 55 (04) :468-479

[5] Mitochondrial dysfunction in autistic patients with 15q inverted duplication [J].

Filipek, PA ;

Juranek, J ;

Smith, M ;

Mays, LZ ;

Ramos, ER ;

Bocian, M ;

Masser-Frye, D ;

Laulhere, TM ;

Modahl, C ;

Spence, MA ;

Gargus, JJ .

ANNALS OF NEUROLOGY, 2003, 53 (06) :801-804

[6] Genetics of autism: Complex aetiology for a heterogeneous disorder [J].

Folstein, SE ;

Rosen-Sheidley, B .

NATURE REVIEWS GENETICS, 2001, 2 (12) :943-955

[7] Epidemiological surveys of autism and other pervasive developmental disorders: An update [J].

Fombonne, E .

JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS, 2003, 33 (04) :365-382

[8]

Gilliam J.E., 1995, Gilliam autism rating scale

[9] Autism associated with the mitochondrial DNA G8363A transfer RNALys mutation [J].

Graf, WD ;

Marin-Garcia, J ;

Gao, HG ;

Pizzo, S ;

Naviaux, RK ;

Markusic, D ;

Barshop, BA ;

Courchesne, E ;

Haas, RH .

JOURNAL OF CHILD NEUROLOGY, 2000, 15 (06) :357-361

[10] SERUM SEROTONIN, LACTATE AND PYRUVATE LEVELS IN INFANTILE AUTISTIC-CHILDREN [J].

LASZLO, A ;

HORVATH, E ;

ECK, E ;

FEKETE, M .

CLINICA CHIMICA ACTA, 1994, 229 (1-2) :205-207

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