Neurology · Neurology / Movement disorders; Neurogenetics
Hereditary spastic paraplegia type 15
also: Kjellin syndrome; SPG15
Recessive HSP with retinal degeneration.
- Specialty
- Neurology
- Subspecialty
- Neurology / Movement disorders; Neurogenetics
- Sex & age distribution
- Male: affected; Female: affected equally; Children: yes, childhood or adolescent onset
- Gene(s) involved
- ZFYVE26
- Alternative names & eponyms
- Kjellin syndrome; SPG15
Etiology & mechanism
ZFYVE26 (spastizin) mutations.
Gene(s) involved (1)
Symptoms & signs (4)
In plain terms, someone with Hereditary spastic paraplegia type 15 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
X-linked adrenoleukodystrophy syndrome
cognitive decline, spastic paraparesis
1 shared
CARASIL
cognitive decline
1 shared
Fragile X-associated tremor/ataxia syndrome
cognitive decline
1 shared
Hereditary spastic paraplegia type 1
spastic paraparesis
1 shared
Hereditary spastic paraplegia type 17
spastic paraparesis
1 shared
Hereditary spastic paraplegia type 20
spastic paraparesis
1 shared
Hereditary spastic paraplegia type 21
spastic paraparesis
1 shared
Hereditary spastic paraplegia type 23
spastic paraparesis
1 shared
Huntington disease phenocopy syndrome
cognitive decline
1 shared
MELAS syndrome
cognitive decline
Shares genes with
None.
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