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.

Oral manifestations in a boy with X-linked reticulate pigmentary disorder

MAGLIONE, MICHELE;
2012-01-01

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.
2012
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11368/2832493
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