Buschke-Ollendorff syndrome
From Wikipedia, the free encyclopedia
Buschke-Ollendorff syndrome Classification and external resources |
|
OMIM | 166700 |
---|---|
DiseasesDB | 30071 |
Buschke-Ollendorff syndrome is a laminopathy associated with LEMD3. It is believed to be inherited in an autosomal dominant manner.[1]
It is named for Abraham Buschke and Helene Ollendorff Curth.[2][3]
[edit] See also
[edit] References
- ^ Online 'Mendelian Inheritance in Man' (OMIM) 166700
- ^ synd/1803 at Who Named It
- ^ A. Buschke, H. Ollendorff-Curth. Ein Fall von Dermatofibrosis lenticularis disseminata und Osteopathia condensans disseminata. Dermatologische Wochenschrift, Hamburg, 1928, 86: 257-262.