Asperger Syndrome, Susceptibility To, 2; Aspg2

Description

Asperger syndrome is considered to be a form of childhood autism (see, e.g., {209850}). The DSM-IV (American Psychiatric Association, 1994) specifies several diagnostic criteria for Asperger syndrome, which has many of the same features as autism. In general, patients with Asperger syndrome and autism exhibit qualitative impairment in social interaction, as manifest by impairment in the use of nonverbal behaviors such as eye-to-eye gaze, facial expression, body postures, and gestures, failure to develop appropriate peer relationships, and lack of social sharing or reciprocity. Patients also exhibit restricted, repetitive and stereotyped patterns of behavior, interests, and activities, including abnormal preoccupation with certain activities and inflexible adherence to routines or rituals. Asperger syndrome is primarily distinguished from autism by the higher cognitive abilities and a more normal and timely development of language and communicative phrases. Gillberg et al. (2001) described the development of the Asperger syndrome (and high-functioning autism) Diagnostic Interview (ASDI), which they claimed has a strong validity in the diagnosis of the disorder.For a discussion of genetic heterogeneity of Asperger syndrome, see ASPG1 (OMIM ).

Clinical Features

Top most frequent phenotypes and symptoms related to Asperger Syndrome, Susceptibility To, 2; Aspg2

  • Absent speech
  • Depressivity
  • Hyperactivity
  • Autism
  • Attention deficit hyperactivity disorder
  • Stereotypy
  • Anorexia
  • Impaired use of nonverbal behaviors
  • Inflexible adherence to routines or rituals
  • Lack of spontaneous play

And another 2 symptoms. If you need more information about this disease we can help you.

Click here to know more about Mendelian.

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
No data available about the known clinical features onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Search Engine

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like RHABDOID TUMOR PREDISPOSITION SYNDROME 1; RTPS1 HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS MULTIPLE EPIPHYSEAL DYSPLASIA DUE TO COLLAGEN 9 ANOMALY EPIDERMOLYSIS BULLOSA, NONSPECIFIC, AUTOSOMAL RECESSIVE; EBNS ZIMMERMANN-LABAND SYNDROME 1; ZLS1 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip; CDG1P ADULT SYNDROME