| Literature DB >> 8457455 |
R Bergman1, O Bitterman-Deutsch, M Fartasch, R Gershoni-Baruch, R Friedman-Birnbaum.
Abstract
Pseudoainhum is an infrequent complication in the autosomal-recessive keratodermas. We describe two related families in which the diagnosis of mal de Meleda keratoderma has been confirmed by mode of inheritance and ultrastructural findings. One family member, a 9-year-old girl, developed pseudoainhum which threatened the viability of her little fingers. This responded to treatment with etretinate. The treatment dilemma posed by keratoderma-induced pseudoainhum in children, i.e. the concern over the possible skeletal toxic effects of long-term etretinate treatment vs. the risks and outcome of surgery, is discussed.Entities:
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Year: 1993 PMID: 8457455 DOI: 10.1111/j.1365-2133.1993.tb15153.x
Source DB: PubMed Journal: Br J Dermatol ISSN: 0007-0963 Impact factor: 9.302