Osteopathia striata with cranial sclerosis and Wilms tumor: Coincidence or consequence?

Clin Genet. 2017 Dec;92(6):674-675. doi: 10.1111/cge.13082.

Authors

F Sperotto¹, G Bisogno¹, E Opocher¹, S Rossi^{2

3}, C Rigon^{2

3}, E Trevisson^{2

3}, F Mercolini¹

Affiliations

¹ Pediatric Hematology and Oncology Unit, Department of Woman's and Child's Health, Padova University, Padova, Italy.
² Institute of Pediatric Research Città della Speranza, Clinical Genetics and Epidemiology Laboratory, Padova University, Padova, Italy.
³ Clinical Genetics Unit, Department of Woman's and Child's Health, University of Padova, Padova, Italy.

PMID: 29120061
DOI: 10.1111/cge.13082

No abstract available

Publication types

Case Reports
Letter
Research Support, Non-U.S. Gov't

MeSH terms

Adaptor Proteins, Signal Transducing / genetics*
Bone Diseases, Developmental / diagnostic imaging
Bone Diseases, Developmental / genetics*
Bone Diseases, Developmental / physiopathology
Child, Preschool
Female
Germ-Line Mutation / genetics
Humans
Loss of Function Mutation / genetics
Osteosclerosis / complications
Osteosclerosis / diagnostic imaging
Osteosclerosis / genetics*
Osteosclerosis / physiopathology
Radiography
Skull / physiopathology
Tumor Suppressor Proteins / genetics*
Wilms Tumor / complications
Wilms Tumor / diagnostic imaging
Wilms Tumor / genetics*
Wilms Tumor / physiopathology

Substances

AMER1 protein, human
Adaptor Proteins, Signal Transducing
Tumor Suppressor Proteins

Supplementary concepts

Osteopathia striata cranial sclerosis