SDHA mutation with dominant transmission results in complex II deficiency with ocular, cardiac, and neurologic involvement. Issue 1 (28th September 2016)

• Record Type: Journal Article
• Authors: Courage, Carolina; Jackson, Christopher B.; Hahn, Dagmar; Euro, Liliya; Nuoffer, Jean‐Marc; Gallati, Sabina; Schaller, André
• Is Part Of: American journal of medical genetics. Volume 173:Issue 1(2017)
• Page Start: 225
• Page End: 230
• Publication Date: 2016-09-28
• Subjects: complex II deficiency -- SDHA -- mitochondrial disorder -- cardiomyopathy -- optic atrophy; Medical genetics -- Periodicals; 616.14205
• DOI: 10.1002/ajmg.a.37986
• Languages: English
• ISSNs: 1552-4825

Abstract

Abstract : Isolated defects of the mitochondrial respiratory complex II (succinate dehydrogenase, SDH) are rare, accounting for approximately 2% of all respiratory chain deficiency diagnoses. Here, we report clinical and molecular investigations of three family members with a heterozygous mutation in the large flavoprotein subunit SDHA previously described to cause complex II deficiency. The index patient presented with bilateral optic atrophy and ocular movement disorder, a progressive polyneuropathy, psychiatric involvement, and cardiomyopathy. Two of his children presented with cardiomyopathy and methylglutaconic aciduria in early childhood. The daughter deceased at the age of 7 months due to cardiac insufficiency. The 30‐year old son presents with cardiomyopathy and developed bilateral optic atrophy in adulthood. Of the four nuclear encoded proteins composing complex II (SDHA, SDHB, SDHC, SDHD) and currently known assembly factors SDHAF1 and SDHAF2 mainly recessively inherited mutations have been described in SDHA, SDHB, SDHD, and SDHAF1 to be causative for mitochondrial disease phenotypes. This is the second report presenting autosomal dominant inheritance of a SDHA mutation.© 2016 Wiley Periodicals, Inc.