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: 
MAGLIONE, MICHELE
mostra contributor esterni 
Data di pubblicazione: 2012
Rivista: 
HEAD & FACE MEDICINE  
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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