Entry - %608638 - ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1; ASPG1 - OMIM
% 608638

ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1; ASPG1


Cytogenetic location: 3q25-q27     Genomic coordinates (GRCh38): 3:149,200,001-188,200,000


Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
3q25-q27 {Asperger syndrome susceptibility 1} 608638 IC, Mu 2
Clinical Synopsis
 
Phenotypic Series
 

INHERITANCE
- Isolated cases
- Multifactorial
NEUROLOGIC
Central Nervous System
- Normal, timely language development
Behavioral Psychiatric Manifestations
- Impaired social interactions
- Impaired use of nonverbal behaviors, such as eye-to-eye gaze, facial expression, body posture, and gestures
- Impaired ability to form peer relationships
- Lack of spontaneous play
- Restrictive behavior, interests, and activities
- Stereotyped, repetitive behavior
- Inflexible adherence to routines or rituals
- Relatively higher cognitive abilities than classic autism (608636)
MISCELLANEOUS
- Onset in early childhood

TEXT

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.

Genetic Heterogeneity of Susceptibility to Asperger Syndrome

ASPG1 maps to chromosome 3q. Other autosomal loci include ASPG2 (608631) on chromosome 17p, ASPG3 (608781) on 1q21-q22, and ASPG4 (609954) on 3p24-p21.


Clinical Features

Asperger (1944) described a syndrome, which he termed 'autistic psychopathy,' in which persons of apparently normal intelligence exhibited an impairment in social interaction and behavioral abnormalities without delays in language development.


Mapping

Auranen et al. (2002) found that in their collection of 38 Finnish families in which a proband had autism, approximately one-third of the probands had a first-degree relative with Asperger syndrome or developmental dysphagia. The authors defined this group as having 'autism spectrum disorders.' In 18 families with both autism and Asperger syndrome, the most significant evidence for linkage was found on chromosome 3q25-q27, with a maximum 2-point lod score of 4.31 at theta = 0.0 with D3S3037.


Population Genetics

Bertrand et al. (2001) performed a prevalence study of autism spectrum disorders in Brick Township, New Jersey. There were 6.7 cases per 1,000 children, aged 3 to 10 years, in 1998. The prevalence for children whose condition met full diagnostic criteria for autistic disorder was 4.0 cases per 1,000 children, and the prevalence for pervasive developmental disorder (PDD)-not otherwise specified (NOS) and Asperger syndrome was 2.7 cases per 1,000 children.


See Also:

REFERENCES

  1. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders. (4th ed.) Washington, D.C.: American Psychiatric Association (pub.) 1994.

  2. Asperger, H. Die 'Autistischen Psychopathen' im Kindesalter. Arch. Psychiatr. Nervenkr. 117: 76-136, 1944.

  3. Auranen, M., Vanhala, R., Varilo, T., Ayers, K., Kempas, E., Ylisaukko-oja, T., Sinsheimer, J. S., Peltonen, L., Jarvela, I. A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27. Am. J. Hum. Genet. 71: 777-790, 2002. [PubMed: 12192642, images, related citations] [Full Text]

  4. Bertrand, J., Mars, A., Boyle, C., Bove, F., Yeargin-Allsopp, M., Decoufle, P. Prevalence of autism in a United States population: the Brick Township, New Jersey, investigation. Pediatrics 108: 1155-1161, 2001. [PubMed: 11694696, related citations] [Full Text]

  5. Gillberg, C., Gillberg, C., Rastam, M., Wentz, E. The Asperger syndrome (and high-functioning autism) Diagnostic Interview (ASDI): a preliminary study of a new structured clinical interview. Autism 5: 57-66, 2001. [PubMed: 11708390, related citations] [Full Text]

  6. Gillberg, C. Asperger syndrome and high-functioning autism. Brit. J. Psychiat. 172: 200-209, 1998. [PubMed: 9614468, related citations] [Full Text]


Creation Date:
Cassandra L. Kniffin : 5/6/2004
carol : 03/03/2023
carol : 07/09/2016
carol : 11/14/2013
carol : 11/14/2013
mcolton : 11/13/2013
carol : 11/8/2013
tkritzer : 7/8/2004
ckniffin : 5/19/2004
ckniffin : 5/18/2004
carol : 5/17/2004
carol : 5/17/2004
carol : 5/17/2004
ckniffin : 5/6/2004

% 608638

ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1; ASPG1


DO: 0050432;  


Cytogenetic location: 3q25-q27     Genomic coordinates (GRCh38): 3:149,200,001-188,200,000


Gene-Phenotype Relationships

Location Phenotype Phenotype
MIM number
Inheritance Phenotype
mapping key
3q25-q27 {Asperger syndrome susceptibility 1} 608638 Isolated cases; Multifactorial 2

TEXT

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.

Genetic Heterogeneity of Susceptibility to Asperger Syndrome

ASPG1 maps to chromosome 3q. Other autosomal loci include ASPG2 (608631) on chromosome 17p, ASPG3 (608781) on 1q21-q22, and ASPG4 (609954) on 3p24-p21.


Clinical Features

Asperger (1944) described a syndrome, which he termed 'autistic psychopathy,' in which persons of apparently normal intelligence exhibited an impairment in social interaction and behavioral abnormalities without delays in language development.


Mapping

Auranen et al. (2002) found that in their collection of 38 Finnish families in which a proband had autism, approximately one-third of the probands had a first-degree relative with Asperger syndrome or developmental dysphagia. The authors defined this group as having 'autism spectrum disorders.' In 18 families with both autism and Asperger syndrome, the most significant evidence for linkage was found on chromosome 3q25-q27, with a maximum 2-point lod score of 4.31 at theta = 0.0 with D3S3037.


Population Genetics

Bertrand et al. (2001) performed a prevalence study of autism spectrum disorders in Brick Township, New Jersey. There were 6.7 cases per 1,000 children, aged 3 to 10 years, in 1998. The prevalence for children whose condition met full diagnostic criteria for autistic disorder was 4.0 cases per 1,000 children, and the prevalence for pervasive developmental disorder (PDD)-not otherwise specified (NOS) and Asperger syndrome was 2.7 cases per 1,000 children.


See Also:

Gillberg (1998)

REFERENCES

  1. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders. (4th ed.) Washington, D.C.: American Psychiatric Association (pub.) 1994.

  2. Asperger, H. Die 'Autistischen Psychopathen' im Kindesalter. Arch. Psychiatr. Nervenkr. 117: 76-136, 1944.

  3. Auranen, M., Vanhala, R., Varilo, T., Ayers, K., Kempas, E., Ylisaukko-oja, T., Sinsheimer, J. S., Peltonen, L., Jarvela, I. A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27. Am. J. Hum. Genet. 71: 777-790, 2002. [PubMed: 12192642] [Full Text: https://doi.org/10.1086/342720]

  4. Bertrand, J., Mars, A., Boyle, C., Bove, F., Yeargin-Allsopp, M., Decoufle, P. Prevalence of autism in a United States population: the Brick Township, New Jersey, investigation. Pediatrics 108: 1155-1161, 2001. [PubMed: 11694696] [Full Text: https://doi.org/10.1542/peds.108.5.1155]

  5. Gillberg, C., Gillberg, C., Rastam, M., Wentz, E. The Asperger syndrome (and high-functioning autism) Diagnostic Interview (ASDI): a preliminary study of a new structured clinical interview. Autism 5: 57-66, 2001. [PubMed: 11708390] [Full Text: https://doi.org/10.1177/1362361301005001006]

  6. Gillberg, C. Asperger syndrome and high-functioning autism. Brit. J. Psychiat. 172: 200-209, 1998. [PubMed: 9614468] [Full Text: https://doi.org/10.1192/bjp.172.3.200]


Creation Date:
Cassandra L. Kniffin : 5/6/2004

Edit History:
carol : 03/03/2023
carol : 07/09/2016
carol : 11/14/2013
carol : 11/14/2013
mcolton : 11/13/2013
carol : 11/8/2013
tkritzer : 7/8/2004
ckniffin : 5/19/2004
ckniffin : 5/18/2004
carol : 5/17/2004
carol : 5/17/2004
carol : 5/17/2004
ckniffin : 5/6/2004