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Peripheral neuropathy with hypomyelination, chronic intestinal pseudo-obstruction and deafness: a developmental
V Pingault1, A Guiochon-Mantel, N Bondurand
1Génétique Moléculaire et Physiopathologie, Inserm U468, and Laboratoire de Biochimie et Génétique, Assistance Publique Hôpitaux de Paris, Hôpital Henri Mondor, Créteil, France.
Abstract:
We describe the case of a girl with an unusual congenital phenotype, combining peculiar peripheral nerve lesions with hypomyelination, chronic intestinal pseudoobstruction, and deafness. She was found to have a de novo heterozygous frameshift mutation in the gene encoding the SOX10 transcription factor. The likely role of SOX10 in determining the fate of Schwann cells during early embryogenesis may explain the peripheral nervous system developmental disorder observed in this patient.
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