Dermochondrocorneal Dystrophy (François' Syndrome): Report of a Case

Ruggero Caputo; Niccla Sambvani; Marcello Monti; Stefano Cavicchini; Antonio Carrassi; Roberto Ratiglia

doi:10.1001/archderm.1988.01670030090029

Dermochondrocorneal Dystrophy (François' Syndrome): Report of a Case

Ruggero Caputo, Niccla Sambvani, Marcello Monti, Stefano Cavicchini, Antonio Carrassi, Roberto Ratiglia

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

Abstract

Dermochondrocorneal dystrophy (François' syndrome) is an extremely rare disorder characterized by firm, nodular lesions involving the hands and the face; osteochondrodystrophy of the peripheral extremital bones, resulting in limitation of movement; and corneal dystrophy marked by white or brownish opacities. A nonfamilial case of dermochondrocorneal dystrophy was studied in a 45-year-old woman who had severe involvement of the gingival and palatal mucous membranes.

Original language	English
Pages (from-to)	424-428
Number of pages	5
Journal	Archives of Dermatology
Volume	124
Issue number	3
DOIs	https://doi.org/10.1001/archderm.1988.01670030090029
Publication status	Published - 1988

ASJC Scopus subject areas

Dermatology

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title = "Dermochondrocorneal Dystrophy (Fran{\c c}ois' Syndrome): Report of a Case",

abstract = "Dermochondrocorneal dystrophy (Fran{\c c}ois' syndrome) is an extremely rare disorder characterized by firm, nodular lesions involving the hands and the face; osteochondrodystrophy of the peripheral extremital bones, resulting in limitation of movement; and corneal dystrophy marked by white or brownish opacities. A nonfamilial case of dermochondrocorneal dystrophy was studied in a 45-year-old woman who had severe involvement of the gingival and palatal mucous membranes.",

author = "Ruggero Caputo and Niccla Sambvani and Marcello Monti and Stefano Cavicchini and Antonio Carrassi and Roberto Ratiglia",

year = "1988",

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language = "English",

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T2 - Report of a Case

AU - Caputo, Ruggero

AU - Sambvani, Niccla

AU - Monti, Marcello

AU - Cavicchini, Stefano

AU - Carrassi, Antonio

AU - Ratiglia, Roberto

PY - 1988

Y1 - 1988

N2 - Dermochondrocorneal dystrophy (François' syndrome) is an extremely rare disorder characterized by firm, nodular lesions involving the hands and the face; osteochondrodystrophy of the peripheral extremital bones, resulting in limitation of movement; and corneal dystrophy marked by white or brownish opacities. A nonfamilial case of dermochondrocorneal dystrophy was studied in a 45-year-old woman who had severe involvement of the gingival and palatal mucous membranes.

AB - Dermochondrocorneal dystrophy (François' syndrome) is an extremely rare disorder characterized by firm, nodular lesions involving the hands and the face; osteochondrodystrophy of the peripheral extremital bones, resulting in limitation of movement; and corneal dystrophy marked by white or brownish opacities. A nonfamilial case of dermochondrocorneal dystrophy was studied in a 45-year-old woman who had severe involvement of the gingival and palatal mucous membranes.

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Dermochondrocorneal Dystrophy (François' Syndrome): Report of a Case

Abstract

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