Buschke-Ollendorff syndrome

Buschke–Ollendorff sign
Buschke–Ollendorff syndrome has an autosomal dominant pattern of inheritance.
Classification and external resources
ICD-10	Q78.8
OMIM	166700
DiseasesDB	30071
MeSH	C537415
Orphanet	1306
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Buschke–Ollendorff syndrome, also known as Dermatofibrosis lenticularis disseminata, is a rare genetic disorder associated with LEMD3. It is believed to be inherited in an autosomal dominant manner.

It is named for Abraham Buschke and Helene Ollendorff Curth who described it in a 45-year-old woman. Its frequency is almost 1 case per every 20,000 people and is equally found in both males and females.

Tenderness on pressure over papular lesions tested with a pin

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