N syndrome

Common Name(s)

N syndrome

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "N syndrome" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "N syndrome" returned 139 free, full-text research articles on human participants. First 3 results:

N-Methyl-D-Aspartate Receptors, Ketamine, and Rett Syndrome: Something Special on the Road to Treatments?
 

Author(s): David M Katz, Frank S Menniti, Robert J Mather

Journal: Biol. Psychiatry. 2016 May;79(9):710-2.

 

Last Updated: 15 Apr 2016

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Structure of the human MLH1 N-terminus: implications for predisposition to Lynch syndrome.
 

Author(s): Hong Wu, Hong Zeng, Robert Lam, Wolfram Tempel, Iain D Kerr, Jinrong Min

Journal: Acta Crystallogr F Struct Biol Commun. 2015 Aug;71(Pt 8):981-5.

 

Mismatch repair prevents the accumulation of erroneous insertions/deletions and non-Watson-Crick base pairs in the genome. Pathogenic mutations in the MLH1 gene are associated with a predisposition to Lynch and Turcot's syndromes. Although genetic testing for these mutations is available, ...

Last Updated: 7 Aug 2015

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Severe dermatitis, multiple allergies, and metabolic wasting syndrome caused by a novel mutation in the N-terminal plakin domain of desmoplakin.
 

Author(s): Maeve A McAleer, Elizabeth Pohler, Frances J D Smith, Neil J Wilson, Christian Cole, Stuart MacGowan, Jennifer L Koetsier, Lisa M Godsel, Robert M Harmon, Robert Gruber, Debra Crumrine, Peter M Elias, Michael McDermott, Karina Butler, Annemarie Broderick, Ofer Sarig, Eli Sprecher, Kathleen J Green, W H Irwin McLean, Alan D Irvine

Journal: J. Allergy Clin. Immunol.. 2015 Nov;136(5):1268-76.

 

Severe dermatitis, multiple allergies, and metabolic wasting (SAM) syndrome is a recently recognized syndrome caused by mutations in the desmoglein 1 gene (DSG1). To date, only 3 families have been reported.

Last Updated: 9 Nov 2015

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "N syndrome" returned 2 free, full-text review articles on human participants. First 3 results:

Use of n-3 PUFAs can decrease the mortality in patients with systemic inflammatory response syndrome: a systematic review and meta-analysis.
 

Author(s): Xiao Wan, Xuejin Gao, Jingcheng Bi, Feng Tian, Xinying Wang

Journal:

 

There have been several meta-analyses evaluating the effect of n-3 polyunsaturated fatty acids (PUFAs) in critically ill patients, but of these, none focused on patients with systemic inflammatory response syndrome (SIRS). The objective of this meta-analysis was to evaluate the effect ...

Last Updated: 20 May 2015

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n-3 fatty acids and the metabolic syndrome.
 

Author(s): Yvon A Carpentier, Laurence Portois, Willy J Malaisse

Journal: Am. J. Clin. Nutr.. 2006 Jun;83(6 Suppl):1499S-1504S.

 

The metabolic syndrome is defined as the coexistence of 3 or more components, some of which indicate alterations in glucose and lipid metabolism. The prevalence of the metabolic syndrome is rapidly increasing in relation to obesity, and it is considered to be an important predictor ...

Last Updated: 17 Jul 2006

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Symptoms, Diagnosis, and Treatment

There are currently no related results available in Genetics Home Reference.

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Clinical Trials of N-acetyl Glucosamine Capsule for IBS-D Treatment
 

Status: Recruiting

Condition Summary: Irritable Bowel Syndrome

 

Last Updated: 17 Jul 2015

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Multicenter Withdrawal Clinical Trials of N-acetyl Glucosamine Capsule for IBS-D Treatment
 

Status: Recruiting

Condition Summary: Irritable Bowel Syndrome

 

Last Updated: 23 Jul 2015

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Congenital Muscle Disease Study of Patient and Family Reported Medical Information
 

Status: Recruiting

Condition Summary: Muscular Dystrophy; Congenital Muscular Dystrophy; Fukutin-related Protein Gene; Limb Girdle; FKRP Gene; Childhood Onset LGMD; Adult Onset LGMD; POMT1; POMT2; POMGnT1; LARGE; Alpha Dystroglycan; Dystroglycanopathy; Centronuclear; Multiminicore; Multicore; Minicore; Congenital Fiber Type Disproportion; Myotubular; Nemaline; Congenital Myopathy; Neuromuscular; Rigid Spine; Phenotype-Genotype Correlation; Cough Assisted Device; Neuromuscular Disease; Respiratory Exacerbation; Invasive Ventilation; Chest Physiotherapy; Congenital Myopathies; Genetic Mutations; Hypertrophic Cardiomyopathy; Wheelchair Use; Cataract; Opthalmoplegia; Ullrich Congenital Muscular Dystrophy; Intermediate Collagen VI Myopathy; Laminin Alpha 2 Related Congenital Muscular Dystrophy; MDC1A; Merosin Deficient Congenital Muscular Dystrophy; Congenital Muscular Dystrophy Undiagnosed; Congenital Muscular Dystrophy Merosin Positive; Walker Warburg Syndrome; Muscle Eye Brain Disease; Fukuyama; Integrin Alpha 7 Deficiency; Integrin Alpha 9 Deficiency; Laminopathy; Lamin AC; SEPN 1 Related Myopathies; Bethlem Myopathy; Dystroglycanopathies; LGMD2K; LGMD2I; LGMD2L; LGMD2N; Actin Aggregation Myopathy; Cap Disease; Central Core Disease; Centronuclear Myopathy; Core Rod Myopathy; Hyaline Body Myopathy; Multiminicore Myopathy; Myotubular Myopathy; Nemaline Myopathy; Tubular Aggregate Myopathy; Zebra Body Disease Myopathy; Congenital Myopathy Other; Reducing Body Myopathy; Sarcotubular Myopathy; Spheroid Body Myopathy

 

Last Updated: 27 Jul 2016

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