Buschke-Ollendorff syndrome due to a novel LEMD3 mutation - an unusual case of alopecia

J Dtsch Dermatol Ges. 2018 Mar;16(3):348-349. doi: 10.1111/ddg.13446. Epub 2018 Feb 21.

Authors

Susanne Darr-Foit¹, Sibylle Schliemann¹, Solveig Schulz², Peter Elsner¹

Affiliations

¹ Department of Dermatology, Jena University Hospital, Jena, Germany.
² Center of Human Genetics, Jena University Hospital, Jena, Germany.

PMID: 29465813
DOI: 10.1111/ddg.13446

No abstract available

Publication types

Letter

MeSH terms

Alopecia / diagnosis*
Alopecia / genetics*
Alopecia / pathology
Biopsy
DNA Mutational Analysis
DNA-Binding Proteins
Diagnosis, Differential
Female
Humans
Membrane Proteins / genetics*
Middle Aged
Nuclear Proteins / genetics*
Osteopoikilosis / diagnosis*
Osteopoikilosis / genetics*
Osteopoikilosis / pathology
Scalp / pathology
Skin Diseases, Genetic / diagnosis*
Skin Diseases, Genetic / genetics*
Skin Diseases, Genetic / pathology

Substances

DNA-Binding Proteins
LEMD3 protein, human
Membrane Proteins
Nuclear Proteins

Supplementary concepts

Buschke-Ollendorff syndrome