X-linked reticulate pigmentary disorder (XLPDR) is a rare, multi-systemic disease with only a limited number of families described in the literature. XLPDR has a genetic origin and the gene has been mapped to Zp22p21. Dental features resemble those of hypohidrotic ectodermal dysplasia. A case of a 3-years-old boy is described.
Titolo: | Oral manifestations in a boy with X-linked reticulate pigmentary disorder |
Autori: | |
Data di pubblicazione: | 2012 |
Rivista: | |
Abstract: | X-linked reticulate pigmentary disorder (XLPDR) is a rare, multi-systemic disease with only a limited number of families described in the literature. XLPDR has a genetic origin and the gene has been mapped to Zp22p21. Dental features resemble those of hypohidrotic ectodermal dysplasia. A case of a 3-years-old boy is described. |
Handle: | http://hdl.handle.net/11368/2832493 |
Appare nelle tipologie: | 1.5 Abstract in Rivista |
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