Tongue Protrusion Dystonia in Pantothenate Kinase-Associated Neurodegeneration

Pediatr Neurol. 2020 Feb:103:76-78. doi: 10.1016/j.pediatrneurol.2019.06.004. Epub 2019 Jun 13.

Abstract

Background: Tongue protrusion dystonia is an uncommon focal dystonia involving the lingual muscles. Causes of tongue protrusion dystonia include tardive dystonia, posthypoxic dystonia, neuroacanthocytosis, pantothenate kinase-associated neurodegeneration, and Lesch-Nyhan syndrome.

Method: We summarize three children with pantothenate kinase-associated neurodegeneration and tongue protrusion dystonia. All three patients underwent careful neurological examination, brain magnetic resonance imaging, and genetic testing.

Results: Tongue protrusion dystonia was a prominent and disabling symptom in all three patients. Brain magnetic resonance imaging revealed a typical eye of the tiger sign in all patients. Two patients had the same genetic mutation (c.1168 A>T mutation, p.I390F).

Conclusions: Tongue protrusion dystonia may be a clue to the underlying etiology of dystonia, including hereditary forms of dystonia. Among them, pantothenate kinase-associated neurodegeneration is an important cause, especially in children.

Keywords: Lingual dystonia; NBIA; Neurodegeneration with brain iron accumulation; PKAN; Pantothenate kinase-associated; Tongue protrusion dystonia.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Child
  • Dystonic Disorders* / diagnosis
  • Dystonic Disorders* / etiology
  • Dystonic Disorders* / genetics
  • Dystonic Disorders* / pathology
  • Female
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Pantothenate Kinase-Associated Neurodegeneration* / complications
  • Pantothenate Kinase-Associated Neurodegeneration* / diagnosis
  • Pantothenate Kinase-Associated Neurodegeneration* / genetics
  • Pantothenate Kinase-Associated Neurodegeneration* / pathology
  • Tongue / physiopathology*