Two sibs with myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders

Am J Med Genet. 1999 Dec 3;87(4):289-93. doi: 10.1002/(sici)1096-8628(19991203)87:4<289::aid-ajmg1>3.0.co;2-t.

Abstract

We present a family with four children born to second-cousin parents. Two of the children had myoclonic epilepsy, congenital deafness, a dystrophic pattern of the macular pigment epithelium, incomplete right bundle branch block, and psychiatric disorders appearing after fever episodes. Results of all laboratory investigations including mitochondrial DNA analysis were normal. Despite the fact that this condition resembles one reported by Latham and Munro in 1937, it is possible that we might be reporting on a new autosomal recessive syndrome.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Bundle-Branch Block / physiopathology
  • Consanguinity
  • Deafness / congenital*
  • Epilepsies, Myoclonic / genetics
  • Epilepsies, Myoclonic / pathology*
  • Family Health
  • Female
  • Humans
  • Macular Degeneration / genetics
  • Macular Degeneration / pathology*
  • Male
  • Mental Disorders / genetics
  • Mental Disorders / pathology*
  • Nuclear Family