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 / Callea, M; Maglione, Michele; Yavuz, I; Deroma, L; Willoughby, Ce; Tadini, G.. - In: HEAD & FACE MEDICINE. - ISSN 1746-160X. - ELETTRONICO. - 2012:8(Suppl 1)(2012), pp. 9-9. [10.1186/1746-160x-8-S1-P9]
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.File in questo prodotto:
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