Dystrophic calcifications point the way-Unusual and early diagnostic clue of Conradi-Hünermann-Happle syndrome

Kenneth Yu; Alexander T Reid; Stephanie J T Chen; Rajiv M Patel; Steven M Donn; Johann E Gudjonsson; Lori Lowe

doi:10.1016/j.jdcr.2017.10.018

Dystrophic calcifications point the way-Unusual and early diagnostic clue of Conradi-Hünermann-Happle syndrome

JAAD Case Rep. 2018 Mar 31;4(4):333-336. doi: 10.1016/j.jdcr.2017.10.018. eCollection 2018 May.

Authors

Kenneth Yu¹, Alexander T Reid², Stephanie J T Chen³, Rajiv M Patel^{1

4}, Steven M Donn⁵, Johann E Gudjonsson¹, Lori Lowe^{1

5}

Affiliations

¹ Department of Dermatology, University of Michigan, Ann Arbor, Michigan.
² University of Michigan School of Medicine, Ann Arbor, Michigan.
³ Department of Pathology, University of Iowa, Iowa City, Iowa.
⁴ Department of Pathology, University of Michigan, Ann Arbor, Michigan.
⁵ Department of Pediatrics, University of Michigan, Ann Arbor, Michigan.

No abstract available

Keywords: Conradi-Hünermann-Happle syndrome; EBP, emopamil-binding protein; chondrodysplasia punctata; congenital ichthyosis; intracorneal calcifications.

Publication types

Case Reports