Compound heterozygous deletions of PMP22 causing severe Charcot-Marie-Tooth disease of the Dejerine-Sottas disease phenotype

Khalid Al-Thihli, Teresa Rudkin, Nancy Carson, Chantal Poulin, Serge Melançon, Vazken M. Der Kaloustian

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

Dejerine-Sottas disease (DSD) is a particular phenotype of the Charcot-Marie-Tooth (CMT) disease spectrum that is genetically heterogeneous. It represents a severe form of hypertrophic axonal and demyelinating neuropathy. Although it is predominantly inherited as an autosomal recessive condition, autosomal dominant inheritance has also been described. To date, the autosomal recessive forms of DSD are classified into several CMT type 4 (CMT4) subclasses based on allelic heterogeneity. We present a 7-year-old boy with a severe form of CMT disease consistent with the autosomal recessive phenotype of DSD. He was found to be a compound heterozygote for mutations in the PMP22 gene resulting in homozygous deletion of exons 2 and 3. The maternally inherited allele was the typical 1.5 Mb deletion involving PMP22 seen with hereditary neuropathy with liability to pressure palsy (HNPP). The paternally inherited allele was a deletion of exons 2 and 3. Both parents presented with a typical clinical picture of HNPP. To our knowledge, this is the first patient reported with large deletions involving both PMP22 alleles. Our patient has also developed severe gastroesophageal reflux disease (GERD), a clinical feature not previously reported with CMT or DSD. The correlation of the phenotype and the molecular defects observed in this patient may set a new subcategory in the classification of DSD.

Original languageEnglish
Pages (from-to)2412-2416
Number of pages5
JournalAmerican Journal of Medical Genetics, Part A
Volume146
Issue number18
DOIs
Publication statusPublished - Sep 15 2008

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Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Phenotype
Alleles
Exons
Tooth
Heterozygote
Gastroesophageal Reflux
Parents
Mutation
Genes

Keywords

  • Charcot-Marie-Tooth disease (CMT)
  • CMT4
  • Dejerine-Sottas disease (DSD)
  • Gastroesophageal reflux disease (GERD)
  • Hereditary neuropathy with liability to pressure palsy (HNPP)
  • Hereditary sensory neuropathy type 1 (HSN 1)
  • PMP22

ASJC Scopus subject areas

  • Genetics(clinical)

Cite this

Compound heterozygous deletions of PMP22 causing severe Charcot-Marie-Tooth disease of the Dejerine-Sottas disease phenotype. / Al-Thihli, Khalid; Rudkin, Teresa; Carson, Nancy; Poulin, Chantal; Melançon, Serge; Der Kaloustian, Vazken M.

In: American Journal of Medical Genetics, Part A, Vol. 146, No. 18, 15.09.2008, p. 2412-2416.

Research output: Contribution to journalArticle

Al-Thihli, Khalid ; Rudkin, Teresa ; Carson, Nancy ; Poulin, Chantal ; Melançon, Serge ; Der Kaloustian, Vazken M. / Compound heterozygous deletions of PMP22 causing severe Charcot-Marie-Tooth disease of the Dejerine-Sottas disease phenotype. In: American Journal of Medical Genetics, Part A. 2008 ; Vol. 146, No. 18. pp. 2412-2416.
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