Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2018Mutation in Na v 1.7 causes high olfactory sensitivity15citations

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Chart of shared publication
Gossrau, G.
1 / 1 shared
Hummel, Thomas
1 / 5 shared
Whitcroft, K. L.
1 / 2 shared
Haehner, Antje
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Krueger, S.
1 / 1 shared
Heinritz, W.
1 / 1 shared
Meinhardt, M.
1 / 1 shared
Chart of publication period
2018

Co-Authors (by relevance)

  • Gossrau, G.
  • Hummel, Thomas
  • Whitcroft, K. L.
  • Haehner, Antje
  • Krueger, S.
  • Heinritz, W.
  • Meinhardt, M.
OrganizationsLocationPeople

article

Mutation in Na v 1.7 causes high olfactory sensitivity

  • Gossrau, G.
  • Sabatowski, R.
  • Hummel, Thomas
  • Whitcroft, K. L.
  • Haehner, Antje
  • Krueger, S.
  • Heinritz, W.
  • Meinhardt, M.
Abstract

<p>Mutations in the sodium-channel Na<sub>v</sub>1.7, encoded by the gene SCN9A, are known to cause pain disorders. In particular, gain-of-function missense mutations in Na<sub>v</sub>1.7 have been shown to be causal in primary erythromelalgia. We present a patient with erythromelalgia, pain attacks and hyperosmia with a mutation within the sodium-channel gene SCN9A. A 50-year-old woman presented with burning pain in both feet and abdominal pain attacks developed over the course of 10 years. Furthermore, this patient experienced a hypersensitivity for odours. Clinical investigation as well as serum/cerebrospinal fluid laboratory findings and electrophysiological testing were unremarkable. Olfactory testing showed high olfactory acuity for all screened modalities and good intranasal sensitivity. Furthermore, quantitative sensory testing within the trigeminal area revealed very low thresholds for thermal, tactile and pain detection. In addition, quantitative sensory testing at the lower legs showed hyperalgesia and, as the disease progresses, thermal sensory function loss. Skin biopsies of the proximal and distal lower limbs revealed reduced epidermal nerve fibre density indicating small fibre neuropathy. Genetic analysis of the SCN9A gene demonstrated a heterozygous mutation in Exon 20 – c.3734A&gt;G (p.N1245S). Treatment with clinically available sodium-channel inhibitors did not result in significant pain relief. Local application of the sodium-channel blocker ambroxol however, reduced pain intensity. Continuous odour exposure stabilised mood and induced a short-term pain relief. This clinical note illustrates the course of middle-age onset erythromelalgia and points to clinical findings related to a likely pathogenic missense mutation affecting the sodium-channel Na<sub>v</sub>1.7. Significance: This case report illustrates the course of middle-age onset erythromelalgia with presumed gain-of-function in olfactory and pain sensation associated with a Nav1.7 channel mutation.</p>

Topics
  • density
  • Sodium