Long-term follow-up of cutaneous changes in siblings with mandibuloacral dysplasia who were originally considered to have hereditary sclerosing poikiloderma.

Published

Journal Article

Mandibuloacral dysplasia is a rare syndrome characterized by mandibular hypoplasia, delayed cranial suture closure, dysplastic clavicles, abbreviated, club-shaped terminal phalanges, acroosteolysis, atrophy of the skin over the hands and feet, and poikilodermatous skin changes. We describe the cases of two siblings with features of mandibuloacral dysplasia who as children were considered to have hereditary sclerosing poikiloderma. On their reevaluation as adults, the clinical features of their condition were perceived to be compatible with mandibuloacral dysplasia.

Full Text

Duke Authors

Cited Authors

  • Fryburg, JS; Sidhu-Malik, N

Published Date

  • November 1995

Published In

Volume / Issue

  • 33 / 5 Pt 2

Start / End Page

  • 900 - 902

PubMed ID

  • 7593806

Pubmed Central ID

  • 7593806

International Standard Serial Number (ISSN)

  • 0190-9622

Digital Object Identifier (DOI)

  • 10.1016/0190-9622(95)90432-8

Language

  • eng

Conference Location

  • United States