Spastic Paraplegia, Hereditary [spastická paraplegie dědičná]
- Terms
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autozomálně dominantní dědičná spastická paraplegie
autozomálně recesivní dědičná spastická paraplegie
dědičná motorická a smyslová neuropatie
dědičná motorická a smyslová neuropatie V
dědičná motoricko-senzorická paraplegie
dědičná recesivní spastická paraplegie vázaná na chromozom X
dědičná spastická paraplegie vázaná na chromozom X
HMSN 5
hypertrofická motoricko-senzorická neuropaticko-spastická paraplegie
spastická paraplegie, typ 2
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Autosomal Dominant Hereditary Spastic Paraplegia
Autosomal Dominant Spastic Paraplegia Hereditary
Autosomal Recessive Hereditary Spastic Paraplegia
Autosomal Recessive Spastic Paraplegia
Autosomal Recessive Spastic Paraplegia, Hereditary
Charcot-Marie-Tooth Disease with Pyramidal Features, Autosomal Dominant
CMT with Pyramidal Features
Hereditary Autosomal Dominant Spastic Paraplegia
Hereditary Autosomal Recessive Spastic Paraplegia
Hereditary Motor and Sensory Neuropathy 5
Hereditary Motor And Sensory Neuropathy V
Hereditary Motor-Sensory Neuropathy with Pyramidal Signs
Hereditary Spastic Paraplegia
Hereditary Spastic Paraplegia, Autosomal Recessive
Hereditary X-Linked Recessive Spastic Paraplegia
Hereditary, Spastic Paraplegia, Autosomal Dominant
Hereditary, Spastic Paraplegia, X-Linked Recessive
HMSN 5
HMSN Type V
HMSN V
HMSN V (Hereditary Motor and Sensory Neuropathy Type V)
Hypertrophic Motor-Sensory Neuropathy-Spastic Paraplegia
Paraplegia, Spastic, Hereditary
Peroneal Muscular Atrophy with Pyramidal Features, Autosomal Dominant
Spastic Paraplegia 2
Spastic Paraplegia Type 2
Spastic Paraplegia Type 5A, Recessive
Spastic Paraplegia-Hypertrophic Motor-Sensory Neuropathy
Spastic Paraplegia, Autosomal Dominant, Hereditary
Spastic Paraplegia, Autosomal Recessive, Hereditary
Spastic Paraplegia, Hereditary, Autosomal Dominant
Spastic Paraplegia, Hereditary, Autosomal Recessive
Spastic Paraplegia, Hereditary, X-Linked Recessive
Spastic Paraplegia, X-Linked Recessive, Hereditary
Type V Hereditary Motor and Sensory Neuropathy
X Linked Recessive Hereditary Spastic Paraplegia
X-linked Recessive Hereditary Spastic Paraplegia
X-Linked, Spastic Paraplegia, Hereditary
A group of inherited diseases that share similar phenotypes but are genetically diverse. Different genetic loci for autosomal recessive, autosomal dominant, and x-linked forms of hereditary spastic paraplegia have been identified. Clinically, patients present with slowly progressive distal limb weakness and lower extremity spasticity. Peripheral sensory neurons may be affected in the later stages of the disease. (J Neurol Neurosurg Psychiatry 1998 Jan;64(1):61-6; Curr Opin Neurol 1997 Aug;10(4):313-8)
- Annotation
- coordinate with GENES, DOMINANT or GENES, RECESSIVE if discussed
- kombinuj s deskriptory GENY DOMINANTNÍ nebo GENY RECESIVNÍ, pokud se o nich hovoří
- DUI
- D015419 MeSH Browser
- CUI
- M0023769
- Previous indexing
- Muscle Spasticity/genetics (1975-1988); Paraplegia/genetics (1966-1988)
- History note
- 1991(1989)
- Public note
- 1991; see NEUROPATHIES, HEREDITARY MOTOR AND SENSORY 1989-1990
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification 1
- CO
- complications 1
- DI
- diagnosis 6
- DG
- diagnostic imaging 2
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology 2
- ET
- etiology
- GE
- genetics 19
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 3
- PP
- physiopathology 2
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy 2
- UR
- urine
- VE
- veterinary
- VI
- virology
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Arena syndrome Disease MeSH Browser
Ataxia, Spastic, 1, Autosomal Dominant Disease MeSH Browser
Ataxia, Spastic, 2, Autosomal Recessive Disease MeSH Browser
Ataxia, Spastic, 3, Autosomal Recessive Disease MeSH Browser
Bahemuka Brown syndrome Disease MeSH Browser
Costeff optic atrophy syndrome Disease MeSH Browser
Fitzsimmons Walson Mellor syndrome Disease MeSH Browser
Fitzsimmons-Guilbert syndrome Disease MeSH Browser
Fitzsimmons-McLachlan-Gilbert syndrome Disease MeSH Browser
Hereditary spastic paralysis, infantile onset ascending Disease MeSH Browser
Leukodystrophy, Dysmyelinating, And Spastic Paraparesis With Or Without Dystonia Disease MeSH Browser
Limb Defects, Distal Transverse, with Mental Retardation and Spasticity Disease MeSH Browser
MASA (Mental Retardation, Aphasia, Shuffling Gait, Adducted Thumbs) Syndrome Disease MeSH Browser
MAST Syndrome Disease MeSH Browser
Mental retardation spasticity ectrodactyly Disease MeSH Browser
Nakamura Osame syndrome Disease MeSH Browser
Roy Maroteaux Kremp syndrome Disease MeSH Browser
Spastic Paraplegia 18, Autosomal Recessive Disease MeSH Browser
Spastic Paraplegia 27, Autosomal Recessive Disease MeSH Browser
Spastic Paraplegia 31, Autosomal Dominant Disease MeSH Browser
Spastic Paraplegia 32, Autosomal Recessive Disease MeSH Browser
Spastic Paraplegia 33, Autosomal Dominant Disease MeSH Browser
Spastic Paraplegia 34, X-Linked Disease MeSH Browser
Spastic Paraplegia 36, Autosomal Dominant Disease MeSH Browser
Spastic Paraplegia 37, Autosomal Dominant Disease MeSH Browser
Spastic Paraplegia 38, Autosomal Dominant Disease MeSH Browser
Spastic Paraplegia 39, Autosomal Recessive Disease MeSH Browser
Spastic Paraplegia 42, Autosomal Dominant Disease MeSH Browser
Spastic Paraplegia 44, Autosomal Recessive Disease MeSH Browser
Spastic Paraplegia 5a, Autosomal Recessive Disease MeSH Browser
Spastic Paraplegia 7, Autosomal Recessive Disease MeSH Browser
Spastic Paraplegia And Evans Syndrome Disease MeSH Browser
Spastic Paraplegia Type 4 Disease MeSH Browser
Spastic Paraplegia Type 7 Disease MeSH Browser
Spastic Paraplegia Type 8 Disease MeSH Browser
Spastic Paraplegia With Associated Extrapyramidal Signs Disease MeSH Browser
Spastic Paraplegia With Myoclonic Epilepsy Disease MeSH Browser
Spastic Paraplegia, Optic Atrophy, And Dementia Disease MeSH Browser
Spastic Paraplegia, Optic Atrophy, Microcephaly, And Xy Sex Reversal Disease MeSH Browser
Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, And Progressive Nephropathy Disease MeSH Browser
Spastic Paraplegia-50, Autosomal Recessive Disease MeSH Browser
Spastic diplegia infantile type Disease MeSH Browser
Spastic paraplegia 10, autosomal dominant Disease MeSH Browser
Spastic paraplegia 11, autosomal recessive Disease MeSH Browser
Spastic paraplegia 12, autosomal dominant Disease MeSH Browser
Spastic paraplegia 13, autosomal dominant Disease MeSH Browser
Spastic paraplegia 14, autosomal recessive Disease MeSH Browser
Spastic paraplegia 15, autosomal recessive Disease MeSH Browser
Spastic paraplegia 16, X-linked Disease MeSH Browser
Spastic paraplegia 17 Disease MeSH Browser
Spastic paraplegia 19, autosomal dominant Disease MeSH Browser
Spastic paraplegia 2, X-linked Disease MeSH Browser
Spastic paraplegia 20, autosomal recessive Disease MeSH Browser
Spastic paraplegia 23 Disease MeSH Browser
Spastic paraplegia 24 Disease MeSH Browser
Spastic paraplegia 25, autosomal recessive Disease MeSH Browser
Spastic paraplegia 26, autosomal recessive Disease MeSH Browser
Spastic paraplegia 29, autosomal dominant Disease MeSH Browser
Spastic paraplegia 3, autosomal dominant Disease MeSH Browser
Spastic paraplegia 4, autosomal dominant Disease MeSH Browser
Spastic paraplegia 6, autosomal dominant Disease MeSH Browser
Spastic paraplegia 9, autosomal dominant Disease MeSH Browser
Spastic paraplegia epilepsy mental retardation Disease MeSH Browser
Spastic paraplegia neuropathy poikiloderma Disease MeSH Browser
Spastic paraplegia type 5B, recessive Disease MeSH Browser
Spastic paraplegia with Kallmann syndrome Disease MeSH Browser
Spastic paraplegia with precocious puberty Disease MeSH Browser
Volcke Soekarman syndrome Disease MeSH Browser