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 |
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Pages (from-to) | 424-428 |
Number of pages | 5 |
Journal | Archives of Dermatology |
Volume | 124 |
Issue number | 3 |
DOIs | |
Publication status | Published - 1988 |
ASJC Scopus subject areas
- Dermatology