Barth syndrome
Barth syndrome | |
OMIM | 302060 |
---|---|
DiseasesDB | 29297 |
WikiDoc Resources for Barth syndrome |
Articles |
---|
Most recent articles on Barth syndrome Most cited articles on Barth syndrome |
Media |
Powerpoint slides on Barth syndrome |
Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on Barth syndrome at Clinical Trials.gov Trial results on Barth syndrome Clinical Trials on Barth syndrome at Google
|
Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on Barth syndrome NICE Guidance on Barth syndrome
|
Books |
News |
Commentary |
Definitions |
Patient Resources / Community |
Patient resources on Barth syndrome Discussion groups on Barth syndrome Patient Handouts on Barth syndrome Directions to Hospitals Treating Barth syndrome Risk calculators and risk factors for Barth syndrome
|
Healthcare Provider Resources |
Causes & Risk Factors for Barth syndrome |
Continuing Medical Education (CME) |
International |
|
Business |
Experimental / Informatics |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Barth syndrome (BTHS), also known as 3-Methylglutaconic aciduria type II and Cardiomyopathy-neutropenia syndrome is a rare genetic disorder classified by many signs and symptoms, including metabolism distortion, delayed motor skills, stamina deficiency, hypotonia, chronic fatigue, delayed growth, cardiomyopathy, and compromised immune system.
Epidemiology and Demographics
It affects at least one hundred families worldwide. Family members of the Barth Syndrome Foundation and its affiliates live in the US, Canada, the UK, Europe, Japan, South Africa, Kuwait, Australia. The syndrome is believed to be severely under-diagnosed and estimated to occur in 1 out of approximately 200,000 births.
The Syndrome was named after Dr. Peter Barth in the Netherlands for his research and discovery in 1983. He described a pedigree chart, showing that this is an inherited trait.
Cause
Mutations in the BTHS gene are associated with cardiolipin molecules in the electron transport chain and the mitochondrial membrane structure. The gene is 6,234 bases in length, mRNA of 879 nucleotides, 11 exons/10 introns, and amino acid sequence of 292 with a weight of 33.5 kDa. It is located at Xq28; the long arm of the X chromosome. Barth Syndrome is caused by 60% frameshift, stop, or splice-site alterations and 30% change in protein's charge.
Barth Syndrome Foundation
The Barth Syndrome Foundation in the US sponsors International Conferences for affected families attending physicians and scientists every two years. The next BSF Conference is presently in the planning stages for summer or fall of 2008. For more information contact the Barth Syndrome Foundation, Inc. at http://www.barthsyndrome.org.
See slso
- 3-Methylglutaconic aciduria
- noncompaction cardiomyopathy: mutations to the affected genes in Barth syndrome are also present here.
External links
- http://www.barthsyndrome.org/ Barth Syndrome Foundation, headed by Shelley Bowen
- NINDS
- http://www.csun.edu/~hcbio033/barth.html
- http://www.hopkinsmedicine.org/cmsl/Barth_Summary.html
- http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Barth+Syndrome