SYNGAP1-Related Intellectual Disability Syndrome

Journal Title: Archives in Neurology & Neuroscience (ANN) - Year 2018, Vol 1, Issue 4

Abstract

SRID Syndrome is a neuro genetic disorder caused by the mutation of the SYNGAP1 gene. This syndrome interferes with the ability to think and properly handle everyday life of a person.

Authors and Affiliations

Keywords

Related Articles

Unmasked Vertigo

Vertigo is a very unpleasant symptom for the patient and a complex clinical problem for the neurologist. First of all: a clear definition is needed, useful for both patients and clinicians and this doesn’t seem a problem...

Neurochemical Effects of Vitamins C, E and DMSO Combinations on Oxidative Stress Biomarkers and Severity of Ischemic Stroke in Wistar Rats

Objective: The objective of this research is to reports the effect of DMSO, Vitamins C and combinations on the oxidative stress biomarkers severity of induced ischemic stroke (IS) in Wistar rats. Materials and methods:...

SYNGAP1-Related Intellectual Disability Syndrome

SRID Syndrome is a neuro genetic disorder caused by the mutation of the SYNGAP1 gene. This syndrome interferes with the ability to think and properly handle everyday life of a person.

Could Abnormal Distribution of Interstitial Cells of Cajal be Involved in Gastrointestinal Disorders in Patients with Parkinson’s Disease?

Objective: To study the role of interstitial cells of Cajal (ICC) in the pathogenesis of gastro-intestinal motility disorders in Parkinson’s disease (PD). Methods: The distribution of ICCs was studied by immunohistochem...

Oculomotor Disorders in Patients with Diabetes

The article focuses on oculomotor disorders in diabetic patients. Quite often diabetic patients have oculomotor neuropathies, both as mononeuropathy and multiple cranial neuropathies. 25% of all cases of paralysis of the...

Download PDF file
  • EP ID EP619985
  • DOI 10.33552/ANN.2018.01.000519
  • Views 102
  • Downloads 0

How To Cite

(2018). SYNGAP1-Related Intellectual Disability Syndrome. Archives in Neurology & Neuroscience (ANN), 1(4), 1-3. https://www.europub.co.uk/articles/-A-619985