Familial hypomelanosis of ito

Pasquale Montagna, G. Procaccianti, G. Gallia, L. Ripamonti, A. Patrizi, A. Baruzzi

Research output: Contribution to journalArticle

Abstract

Two siblings presented the typical skin changes of hypomelanosis of Ito (HI) associated with mental and cerebellar signs. Their mother showed only the skin changes of HI but no neurological disturbances. HI is a hereditary disorder, in which familiarity may go unnoticed because of the different expressions of neural and cutaneous features.

Original languageEnglish
Pages (from-to)345-347
Number of pages3
JournalEuropean Neurology
Volume31
Issue number6
DOIs
Publication statusPublished - 1991

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Hypopigmentation
Skin

Keywords

  • Cerebellar ataxia
  • Hypomelanosis
  • Ito’s syndrome
  • Neurocutaneous syndromes

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology

Cite this

Montagna, P., Procaccianti, G., Gallia, G., Ripamonti, L., Patrizi, A., & Baruzzi, A. (1991). Familial hypomelanosis of ito. European Neurology, 31(6), 345-347. https://doi.org/10.1159/000116690

Familial hypomelanosis of ito. / Montagna, Pasquale; Procaccianti, G.; Gallia, G.; Ripamonti, L.; Patrizi, A.; Baruzzi, A.

In: European Neurology, Vol. 31, No. 6, 1991, p. 345-347.

Research output: Contribution to journalArticle

Montagna, P, Procaccianti, G, Gallia, G, Ripamonti, L, Patrizi, A & Baruzzi, A 1991, 'Familial hypomelanosis of ito', European Neurology, vol. 31, no. 6, pp. 345-347. https://doi.org/10.1159/000116690
Montagna P, Procaccianti G, Gallia G, Ripamonti L, Patrizi A, Baruzzi A. Familial hypomelanosis of ito. European Neurology. 1991;31(6):345-347. https://doi.org/10.1159/000116690
Montagna, Pasquale ; Procaccianti, G. ; Gallia, G. ; Ripamonti, L. ; Patrizi, A. ; Baruzzi, A. / Familial hypomelanosis of ito. In: European Neurology. 1991 ; Vol. 31, No. 6. pp. 345-347.
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