Catalog

Familial multiple lipomata

No MMS code

Link to WHO Definition

Familial multiple lipomata – http://id.who.int/icd/entity/950217777

This autosomal dominant inherited condition is characterised by the development during or soon after adolescence of multiple small, well-demarcated, encapsulated lipomata, typically involving the extremities. In contrast to benign symmetrical lipomatosis the neck and shoulders usually are spared.