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Buschke-Ollendorff Syndrome

Congenital Malformations and Chromosomal Abnormalities

Buschke-Ollendorff syndrome is a rare genetic skin disorder associated with the LEMD3 gene that typically presents with widespread, painless skin papules.

Facts
Classification
Body System
Integumentary System 1
ICD-10 Chapter
XVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 2
Communicable or Non-communicable
Non-Communicable 3
Transmission Route
Non-Transmissible 1
Causative Agent
Causative Agent (category)
Genetic / Hereditary 1
First Described
1928 1
Sources
1. Wikipedia: Buschke-Ollendorff syndrome
Wikipedia
  • Lead: causative agent category
    Buschke-Ollendorff syndrome (BOS) is a rare genetic skin disorder associated with LEMD3 that typically presents with widespread painless papules.
  • Lead section (first-described-year)
    It is named for Abraham Buschke and Helene Ollendorff Curth, who described the condition in one female in 1928.
  • Lead section, body-system statement
    Buschke-Ollendorff syndrome (BOS) is a rare genetic skin disorder associated with LEMD3 that typically presents with widespread painless papules.
  • Lead section, transmission-route statement
    It is inherited in an autosomal dominant manner.
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2. Wikipedia: ICD-10
WikipediaList of chapters, Chapter XVII
Quote, List of chapters, Chapter XVII
Congenital malformations, deformations and chromosomal abnormalities
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3. Wikipedia: Non-communicable disease
WikipediaInherited/genetic diseases section
Quote, Inherited/genetic diseases section
Genetic disorders are caused by errors in genetic information that produce diseases in the affected people.
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