Literature DB >> 7523664

Oro-dental self-mutilation in familial dysautonomia.

E Mass1, N Gadoth.   

Abstract

Orodental self-mutilation (ODSM) has not gained sufficient recognition in familial dysautonomia (FD). Among 38 patients with FD, ODSM was found in 14 (36.8%). ODSM may be due to peripheral neuropathy with insensibility to pain, which is characteristic of FD. Elimination of the sharp edges of teeth was found to be helpful.

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Year:  1994        PMID： 7523664     DOI： 10.1111/j.1600-0714.1994.tb00058.x

Source DB:  PubMed          Journal:  J Oral Pathol Med        ISSN： 0904-2512            Impact factor:   4.253


  5 in total

1.  Case report: A unique presentation of severe tongue biting in 10 month-old twins with a novel approach to management.

Authors:  A Suchak; M Mars
Journal:  Eur Arch Paediatr Dent       Date:  2010-06

Review 2.  Respiratory care in familial dysautonomia: Systematic review and expert consensus recommendations.

Authors:  Mikhail Kazachkov; Jose-Alberto Palma; Lucy Norcliffe-Kaufmann; Bat-El Bar-Aluma; Christy L Spalink; Erin P Barnes; Nancy E Amoroso; Stamatela M Balou; Shay Bess; Arun Chopra; Rany Condos; Ori Efrati; Kathryn Fitzgerald; David Fridman; Ronald M Goldenberg; Ayelet Goldhaber; David A Kaufman; Sanjeev V Kothare; Jeremiah Levine; Joseph Levy; Anthony S Lubinsky; Channa Maayan; Libia C Moy; Pedro J Rivera; Alcibiades J Rodriguez; Gil Sokol; Mark F Sloane; Tina Tan; Horacio Kaufmann
Journal:  Respir Med       Date:  2018-06-21       Impact factor: 3.415

3.  Brainstem reflexes in patients with familial dysautonomia.

Authors:  Joel V Gutiérrez; Lucy Norcliffe-Kaufmann; Horacio Kaufmann
Journal:  Clin Neurophysiol       Date:  2014-07-03       Impact factor: 3.708

4.  Oral self-injuries: clinical findings in a series of 19 patients.

Authors:  Rosangela Cannavale; Angelo Itro; Giuseppina Campisi; Domenico Compilato; Giuseppe Colella
Journal:  Med Oral Patol Oral Cir Bucal       Date:  2015-03-01

Review 5.  Oral manifestations, dental management, and a rare homozygous mutation of the PRDM12 gene in a boy with hereditary sensory and autonomic neuropathy type VIII: a case report and review of the literature.

Authors:  Karim Elhennawy; Seif Reda; Christian Finke; Luitgard Graul-Neumann; Paul-Georg Jost-Brinkmann; Theodosia Bartzela
Journal:  J Med Case Rep       Date:  2017-08-15
  5 in total

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