Autosomal Dominant Spastic Paraplegia Type 19
Autosomal dominant spastic paraplegia type 19 is a pure form of hereditary spastic paraplegia characterized by a slowly progressive and relatively benign spastic paraplegia presenting in adulthood with spastic gait, lower limb hyperreflexia, extensor plantar responses, bladder dysfunction (urinary urgency and/or incontinence), and mild sensory and motor peripheral neuropathy.
Genes related to Autosomal Dominant Spastic Paraplegia Type 19
Clinical FeaturesTop most frequent phenotypes and symptoms related to Autosomal Dominant Spastic Paraplegia Type 19
- Babinski sign
- Difficulty walking
- Spastic paraplegia
- Lower limb muscle weakness
- Muscle cramps
And another 24 symptoms. If you need more information about this disease we can help you.
Incidence and onset information— Based on the latest data available there are 1 families with AUTOSOMAL DOMINANT SPASTIC PARAPLEGIA TYPE 19 in Europe.
— No data available about the known clinical features onset.
Autosomal Dominant Spastic Paraplegia Type 19 Is also known as spg19.
Researches and researchersCurrently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.
Sources and references
You can check the following sources for additional information.ORPHANET OMIM MESH Rare Disease Search Engine
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