Cardiomyopathy-hypotonia-lactic acidosis syndrome

Cardiomyopathy-hypotonia-lactic acidosis syndrome is characterized by hypertrophic cardiomyopathy, muscular hypotonia and the presence of lactic acidosis at birth. It has been described in two sisters (both of whom died within the first year of life) from a nonconsanguineous Turkish family. The syndrome is caused by a homozygous point mutation in the exon 3A of the SLC25A3 gene encoding a mitochondrial membrane transporter.

Also known as: hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome, Mpcd, mitochondrial phosphate carrier deficiency

20 clinical trials for this condition and its sub-types.