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Hereditary spastic paraplegia 61

rare

A rare, complex form of hereditary spastic paraplegia characterized by an onset in infancy of spastic paraplegia (presenting with the inability to walk unsupported and a scissors gait) associated with a motor and sensory polyneuropathy with loss of terminal digits and acropathy. SPG61 is due to a mutation in the ARL6IP1 gene (16p12-p11.2) encoding the ADP-ribosylation factor-like protein 6-interacting protein 1.

Identifiers
MONDO:0014304 OMIM:615685Orphanet:401780
Causal genes
ARL6IP1
Part of
Complex hereditary spastic paraplegia
Also known as
ARL6IP1 autosomal recessive complex spastic paraplegia · autosomal recessive complex spastic paraplegia caused by mutation in ARL6IP1 · autosomal recessive spastic paraplegia type 61 · hereditary spastic paraplegia type 61 · spastic paraplegia 61, autosomal recessive

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