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Lack of Association between Parental ABO Blood Type and Autism Spectrum Disorders.

18:18 EDT 19th June 2013 | BioPortfolio

Summary of "Lack of Association between Parental ABO Blood Type and Autism Spectrum Disorders."

No Summary Available

Affiliation

 Department of Pharmacology, Second Military Medical University, Shanghai, China  Department of Nursing, Second Military Medical University, Shanghai, China  Department of Neurology, Shanghai Hospital, Shanghai, China  Department of Physiology, Se

Journal Details

This article was published in the following journal.

Name: CNS neuroscience & therapeutics
ISSN: 1755-5949
Pages:

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Medical and Biotech [MESH] Definitions

Asperger Syndrome

A childhood disorder predominately affecting boys and similar to autism (AUTISTIC DISORDER). It is characterized by severe, sustained, clinically significant impairment of social interaction, and restricted repetitive and stereotyped patterns of behavior. In contrast to autism, there are no clinically significant delays in language or cognitive development. (From DSM-IV)

Arteriovenous Malformations

Abnormal formation of blood vessels that shunt arterial blood directly into veins without passing through the CAPILLARIES. They usually are crooked, dilated, and with thick vessel walls. A common type is the congenital arteriovenous fistula. The lack of blood flow and oxygen in the capillaries can lead to tissue damage in the affected areas.

Ischemic Contracture

A type of permanent damage to muscles and nerves that results from prolonged lack blood flow to those tissues. It is characterized by shortening and stiffening of the muscles.

Hyperlipoproteinemia Type I

An inherited condition due to a deficiency of either LIPOPROTEIN LIPASE or APOLIPOPROTEIN C-II (a lipase-activating protein). The lack of lipase activities results in inability to remove CHYLOMICRONS and TRIGLYCERIDES from the blood which has a creamy top layer after standing.

Myosin Type I

A subclass of myosins found generally associated with actin-rich membrane structures such as filopodia. Members of the myosin type I family are ubiquitously expressed in eukaryotes. The heavy chains of myosin type I lack coiled-coil forming sequences in their tails and therefore do not dimerize.

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