Neurology · Neurology / Movement disorders; Neurogenetics
Hereditary spastic paraplegia type 17
also: Silver syndrome; SPG17
Dominant HSP with distal amyotrophy.
- Specialty
- Neurology
- Subspecialty
- Neurology / Movement disorders; Neurogenetics
- Sex & age distribution
- Male: affected; Female: affected equally; Children: onset in adolescence to adulthood
- Gene(s) involved
- BSCL2
- Alternative names & eponyms
- Silver syndrome; SPG17
Etiology & mechanism
BSCL2 seipin mutations.
Gene(s) involved (1)
Symptoms & signs (3)
In plain terms, someone with Hereditary spastic paraplegia type 17 may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
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Shares symptoms with
2 shared
Hereditary spastic paraplegia type 20
distal amyotrophy, spastic paraparesis
1 shared
Hereditary spastic paraplegia type 1
spastic paraparesis
1 shared
Hereditary spastic paraplegia type 15
spastic paraparesis
1 shared
Hereditary spastic paraplegia type 21
spastic paraparesis
1 shared
Hereditary spastic paraplegia type 23
spastic paraparesis
1 shared
Triple H syndrome
spastic paraparesis
1 shared
X-linked adrenoleukodystrophy syndrome
spastic paraparesis
Shares genes with
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