[Thévenard ulcero-mutilating acro-osteopathy syndrome]

A 20-year old female patient with characteristic symptoms of acroosteolysis of the left foot (sensory neuropathy, ulcers and hyperkeratosis on the acra, acroosteolysis and peroneal muscleatrophy) is described. The syndrome manifested in early childhood, heridity could not be found. Correspondence to the familial type of acroosteolysis (of Thevenard) as a new mutation is discussed.