| Descriptor English: | Spastic Paraplegia, Hereditary | ||||||
| Descriptor Spanish: |
Paraplejía Espástica Hereditaria
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| Descriptor Portuguese: | Paraplegia Espástica Hereditária | ||||||
| Descriptor French: | Paraplégie spasmodique héréditaire | ||||||
| Entry term(s): |
Autosomal Dominant Hereditary Spastic Paraplegia Autosomal Dominant Spastic Paraplegia Hereditary Autosomal Recessive Hereditary Spastic Paraplegia Autosomal Recessive Spastic Paraplegia, Hereditary CMT with Pyramidal Features Charcot Marie Tooth Disease with Pyramidal Features, Autosomal Dominant Charcot-Marie-Tooth Disease with Pyramidal Features, Autosomal Dominant HMSN 5 HMSN Type V HMSN V HMSN V (Hereditary Motor and Sensory Neuropathy Type V) Hereditary Autosomal Dominant Spastic Paraplegia Hereditary Autosomal Recessive Spastic Paraplegia Hereditary Motor And Sensory Neuropathy V Hereditary Motor Sensory Neuropathy with Pyramidal Signs Hereditary Motor and Sensory Neuropathy 5 Hereditary Motor-Sensory Neuropathy with Pyramidal Signs Hereditary Spastic Paraplegia Hereditary Spastic Paraplegia, Autosomal Recessive Hereditary Spastic Paraplegias Hereditary X Linked Recessive Spastic Paraplegia Hereditary X-Linked Recessive Spastic Paraplegia Hereditary, Spastic Paraplegia, Autosomal Dominant Hereditary, Spastic Paraplegia, X-Linked Recessive Hypertrophic Motor Sensory Neuropathy Spastic Paraplegia Hypertrophic Motor-Sensory Neuropathy-Spastic Paraplegia Paraplegia, Hereditary Spastic Paraplegia, Spastic, Hereditary Paraplegias, Hereditary Spastic Peroneal Muscular Atrophy with Pyramidal Features, Autosomal Dominant Spastic Paraplegia 2 Spastic Paraplegia Hypertrophic Motor Sensory Neuropathy Spastic Paraplegia Type 2 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 Spastic Paraplegia-Hypertrophic Motor-Sensory Neuropathy Spastic Paraplegias, Hereditary Type V Hereditary Motor and Sensory Neuropathy Type V, HMSN X Linked Recessive Hereditary Spastic Paraplegia X-Linked, Spastic Paraplegia, Hereditary X-linked Recessive Hereditary Spastic Paraplegia |
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| Tree number(s): |
C10.500.300.820 C10.574.500.495.820 C10.668.829.800.300.820 C16.131.666.300.820 C16.320.400.375.820 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D015419 | ||||||
| Scope note: | 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) |
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| Annotation: | coordinate with GENES, DOMINANT or GENES, RECESSIVE if discussed |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Muscle Spasticity/genetics (1975-1988) Paraplegia/genetics (1966-1988) |
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| Public MeSH Note: | 1991; see NEUROPATHIES, HEREDITARY MOTOR AND SENSORY 1989-1990 |
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| History Note: | 1991(1989) |
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| DeCS ID: | 23835 | ||||||
| Unique ID: | D015419 | ||||||
| NLM Classification: | WE 550 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1991/01/01 | ||||||
| Date of Entry: | 1988/06/07 | ||||||
| Revision Date: | 2019/05/21 |
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Spastic Paraplegia, Hereditary
- Preferred
X-Linked, Spastic Paraplegia, Hereditary
- Narrower
Hereditary X-Linked Recessive Spastic Paraplegia
- Narrower
Autosomal Recessive Hereditary Spastic Paraplegia
- Narrower
Hereditary Autosomal Dominant Spastic Paraplegia
- Narrower
Hereditary Motor-Sensory Neuropathy with Pyramidal Signs
- Narrower
| Concept UI |
M0023769 |
| Scope note | 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) |
| Preferred term | Spastic Paraplegia, Hereditary |
| Entry term(s) |
Hereditary Spastic Paraplegia Hereditary Spastic Paraplegias Hypertrophic Motor Sensory Neuropathy Spastic Paraplegia Hypertrophic Motor-Sensory Neuropathy-Spastic Paraplegia Paraplegia, Hereditary Spastic Paraplegia, Spastic, Hereditary Paraplegias, Hereditary Spastic Spastic Paraplegia Hypertrophic Motor Sensory Neuropathy Spastic Paraplegia-Hypertrophic Motor-Sensory Neuropathy Spastic Paraplegias, Hereditary |
| Concept UI |
M0336727 |
| Preferred term | X-Linked, Spastic Paraplegia, Hereditary |
| Concept UI |
M0336728 |
| Preferred term | Hereditary X-Linked Recessive Spastic Paraplegia |
| Entry term(s) |
Hereditary X Linked Recessive Spastic Paraplegia Hereditary, Spastic Paraplegia, X-Linked Recessive Spastic Paraplegia 2 Spastic Paraplegia Type 2 Spastic Paraplegia, Hereditary, X-Linked Recessive Spastic Paraplegia, X-Linked Recessive, Hereditary X Linked Recessive Hereditary Spastic Paraplegia X-linked Recessive Hereditary Spastic Paraplegia |
| Concept UI |
M0336750 |
| Preferred term | Autosomal Recessive Hereditary Spastic Paraplegia |
| Entry term(s) |
Autosomal Recessive Spastic Paraplegia, Hereditary Hereditary Autosomal Recessive Spastic Paraplegia Hereditary Spastic Paraplegia, Autosomal Recessive Spastic Paraplegia, Autosomal Recessive, Hereditary Spastic Paraplegia, Hereditary, Autosomal Recessive |
| Concept UI |
M0336734 |
| Preferred term | Hereditary Autosomal Dominant Spastic Paraplegia |
| Entry term(s) |
Autosomal Dominant Hereditary Spastic Paraplegia Autosomal Dominant Spastic Paraplegia Hereditary Charcot Marie Tooth Disease with Pyramidal Features, Autosomal Dominant Charcot-Marie-Tooth Disease with Pyramidal Features, Autosomal Dominant Hereditary, Spastic Paraplegia, Autosomal Dominant Peroneal Muscular Atrophy with Pyramidal Features, Autosomal Dominant Spastic Paraplegia, Autosomal Dominant, Hereditary Spastic Paraplegia, Hereditary, Autosomal Dominant |
| Concept UI |
M000648472 |
| Preferred term | Hereditary Motor-Sensory Neuropathy with Pyramidal Signs |
| Entry term(s) |
CMT with Pyramidal Features HMSN 5 HMSN Type V HMSN V HMSN V (Hereditary Motor and Sensory Neuropathy Type V) Hereditary Motor And Sensory Neuropathy V Hereditary Motor Sensory Neuropathy with Pyramidal Signs Hereditary Motor and Sensory Neuropathy 5 Type V Hereditary Motor and Sensory Neuropathy Type V, HMSN |
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