Agent Commons Collaborative Research

Sterol carrier protein 2 deficiency

rare

A 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.

Causal genes
SCP2
Also known as
leukoencephalopathy - dystonia - motor neuropathy · leukoencephalopathy-dystonia-motor neuropathy syndrome · LKDMN · SCP2 deficiency

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