A Novel GJC2 Mutation Associated with Hypomyelination and Mullerian Agenesis Syndrome: Coincidence or a New Entity?


Yalcinkaya C., Erturk O., Tuysuz B., Yesil G. , Verbeke J. I. M. L. , Keyser B., et al.

NEUROPEDIATRICS, cilt.43, ss.159-161, 2012 (SCI İndekslerine Giren Dergi)

  • Cilt numarası: 43 Konu: 3
  • Basım Tarihi: 2012
  • Doi Numarası: 10.1055/s-0032-1313912
  • Dergi Adı: NEUROPEDIATRICS
  • Sayfa Sayısı: ss.159-161

Özet

In recent years, several new white matter diseases have been identified based on magnetic resonance imaging and clinical findings. For most newly defined disorders the genetic basis has been identified. However, there is still a large group of patients without a specific diagnosis. Hypomyelinating leukodystrophies are the largest group among them. In some disorders characterized by hypomyelination only central nervous system involvement is observed, but in some disorders involvement of other organs is observed as well, such as eyes or teeth. Pelizaeus-Merzbacher-like disease (PMLD) is an autosomal recessive hypomyelinating disorder of the central nervous system characterized by nystagmus, ataxia, and progressive spasticity. The disease is caused by mutations in GJC2, the gene that encodes the gap junction protein connexin 47. Here we describe hypomyelination and Mullerian agenesis syndrome in a girl who is homozygous for a novel mutation in the GJC2 gene. It is an open question whether this is an association by chance or a feature of PMLD not previously noted.