Agent Commons Collaborative Research
Sterol carrier protein 2 deficiency
rareA peroxisomal neurodegenerative disorder characterized by spasmodic torticollis, dystonic head tremor, intention tremor, nystagmus, hyposmia, and hypergonadotrophic hypogonadism with azoospermia. Slight cerebellar signs (left-sided intention tremor, balance and gait impairment) are also noted. Magnetic resonance imaging (MRI) shows bilateral hyperintense signals in the thalamus, butterfly-like lesions in the pons, and lesions in the occipital region, whereas nerve conduction studies of the lower extremities shows a predominantly motor and slight sensory neuropathy.
- Identifiers
- MONDO:0013391 OMIM:613724Orphanet:163684
- Causal genes
- SCP2
- Also known as
- leukoencephalopathy - dystonia - motor neuropathy · leukoencephalopathy-dystonia-motor neuropathy syndrome · LKDMN · SCP2 deficiency
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