Delayed Myelination

Common Name(s)

Delayed Myelination

Description for this condition is not yet available.
 

Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Delayed Myelination" for support, advocacy or research.

KCNQ2 Cure Alliance

The mission of KCNQ2 Cure Alliance is to educate and to advance research leading to treatments or a cure for patients living with the genetic disorder KCNQ2 Epilepsy.

Last Updated: 12 Dec 2015

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General Support Organizations

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Delayed Myelination" for support, advocacy or research.

KCNQ2 Cure Alliance

The mission of KCNQ2 Cure Alliance is to educate and to advance research leading to treatments or a cure for patients living with the genetic disorder KCNQ2 Epilepsy.

http://www.kcnq2cure.org/

Last Updated: 12 Dec 2015

View Details

 

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 "Delayed Myelination" returned 2 free, full-text research articles on human participants. First 3 results:

MCT8 deficiency: extrapyramidal symptoms and delayed myelination as prominent features.
 

Author(s): Davide Tonduti, Adeline Vanderver, Angela Berardinelli, Johanna L Schmidt, Christin D Collins, Francesca Novara, Antonia Di Genni, Alda Mita, Fabio Triulzi, Janice E Brunstrom-Hernandez, Orsetta Zuffardi, Umberto Balottin, Simona Orcesi

Journal: J. Child Neurol.. 2013 Jun;28(6):795-800.

 

Monocarboxylate transporter 8 (MCT8) deficiency is an X-linked disorder resulting from an impairment of the transcellular transportation of thyroid hormones. Within the central nervous system thyroid hormone transport is normally mediated by MCT8. Patients are described as affected ...

Last Updated: 16 May 2013

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Schizophrenia, myelination, and delayed corollary discharges: a hypothesis.
 

Author(s): Thomas J Whitford, Judith M Ford, Daniel H Mathalon, Marek Kubicki, Martha E Shenton

Journal: Schizophr Bull. 2012 May;38(3):486-94.

 

Any etiological theory of schizophrenia must account for at least 3 distinctive features of the disorder, namely its excessive dopamine neurotransmission, its frequent periadolescent onset, and its bizarre, pathognomonic symptoms. In this article, we theorize that each of these features ...

Last Updated: 20 Apr 2012

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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 "Delayed Myelination" returned 1 free, full-text review articles on human participants. First 3 results:

Compound heterozygous variants in PGAP1 causing severe psychomotor retardation, brain atrophy, recurrent apneas and delayed myelination: a case report and literature review.
 

Author(s): Matthias Kettwig, Orly Elpeleg, Eike Wegener, Steffi Dreha-Kulaczewski, Marco Henneke, Jutta Gärtner, Peter Huppke

Journal:

 

Mutations in proteins involved in the glycosylphosphatidylinositol anchor biosynthesis and remodeling pathway are associated with autosomal recessive forms of intellectual disability. Recently mutations in the PGAP1 gene that codes for PGAP1, a protein localized in the endoplasmic ...

Last Updated: 21 May 2016

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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.