Cookies help us deliver our services. By using our services, you agree to our use of cookies. More information

Barth Syndome

From Bioblast


high-resolution terminology - matching measurements at high-resolution


Barth Syndome

Description

Barth Syndome (BTHS) is an X-linked genetic condition that is caused by a mutation in the tafazzin gene (taz). This mutation causes cardiolipin abnormalities, cardiomyopathy, neutropenia, muscle weakness, growth delay, and exercise intolerance.

Weblink

Contributed by Sparagna GC 2016-04-24

Abbreviation: BTHS