Abstract
We report on a case of a now 2-years-old child with pachyonychia congenita syndrome, a rare genodermatosis inherited as an autosomal dominant trait with variable expressivity and high penetrance. In our case there is no family history concerning this inherited disorder so a new mutation is likely. Mutational analysis is under current investigation.
| Translated title of the contribution | Pachyonychia congenita type Jadassohn Lewandowsky |
|---|---|
| Original language | German |
| Pages (from-to) | 861-862 |
| Number of pages | 2 |
| Journal | H+G Zeitschrift fur Hautkrankheiten |
| Volume | 73 |
| Issue number | 12 |
| State | Published - 1998 |