A 19-year old male developed within 5 years a slowly progressive and g
eneralised painless atrophy of the foreleg with a club-tip foot. Initi
ally an undefined bone disease was diagnosed. The first neurologic dia
gnostic procedure led to the tentative diagnosis of post-polio syndrom
e or chronic asymmetrical spinal muscular atrophy. However, after path
ological SSEPs, lumbar magnetic resonance tomography showed a tethered
cord syndrome with a huge intraspinal lipoma. Typically, the tethered
-cord syndrome is combined with congenital malformations and leads to
a conus syndrome with bilateral symptoms. Assuming unilateral symptoms
, the lack of pain or vegetative symptoms, isolated atrophy and atypic
al EMG findings, the diagnosis had been misled.