tellmegen logo

INHERITED MONOGENIC DISEASES

           

Dihydrolipoamide dehydrogenase deficiency

Pyruvate dehydrogenase deficiency (PDHD) is a rare neurometabolic disorder characterized by a wide range of clinical signs with metabolic and neurological components of varying severity. Manifestations range from often fatal, severe, neonatal lactic acidosis to later-onset neurological disorders.

The disorder is caused by mutations in the DLD gene (7q31-q32). The pattern of inheritance is autosomal recessive. The main mutation is c.685G>T (p.Gly229Cys). In the Ashkenazi Jewish population, the carrier frequency of this pathogenic variant is estimated between 1/94 and 1/110 with an estimated disease frequency of 1/35,000 to 1/48,000.

GENE OR REGION STUDIED


  • DLD

CYBER MONDAY

The best deals of 2021

Use our discount codes Only until November 30th!

CYBER MONDAY

Use our discount codes

Only until November 30th!

BUY NOW!