Familial hypomelanosis of ito

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

doi:10.1159/000116690

Familial hypomelanosis of ito

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

Istituto Scienze Neurologiche

Research output: Contribution to journal › Article › peer-review

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 language	English
Pages (from-to)	345-347
Number of pages	3
Journal	European Neurology
Volume	31
Issue number	6
DOIs	https://doi.org/10.1159/000116690
Publication status	Published - 1991

Keywords

Cerebellar ataxia
Hypomelanosis
Ito’s syndrome
Neurocutaneous syndromes

ASJC Scopus subject areas

Clinical Neurology
Neurology

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10.1159/000116690

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title = "Familial hypomelanosis of ito",

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.",

keywords = "Cerebellar ataxia, Hypomelanosis, Ito{\textquoteright}s syndrome, Neurocutaneous syndromes",

author = "Pasquale Montagna and G. Procaccianti and G. Gallia and L. Ripamonti and A. Patrizi and A. Baruzzi",

year = "1991",

doi = "10.1159/000116690",

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AU - Montagna, Pasquale

AU - Procaccianti, G.

AU - Gallia, G.

AU - Ripamonti, L.

AU - Patrizi, A.

AU - Baruzzi, A.

PY - 1991

Y1 - 1991

N2 - 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.

AB - 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.

KW - Cerebellar ataxia

KW - Hypomelanosis

KW - Ito’s syndrome

KW - Neurocutaneous syndromes

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Familial hypomelanosis of ito

Abstract

Keywords

ASJC Scopus subject areas

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