Living with Hereditary spastic paraplegia 14
A type of hereditary spastic paraplegia that starts in adulthood, with stiff legs and mild learning difficulty.
Understanding Hereditary spastic paraplegia 14
Features include stiff legs, a spastic walk, brisk reflexes, high-arched feet, and mild intellectual disability. It also involves nerve damage that affects movement. It starts in adulthood.
Signs & symptoms
Symptoms vary from person to person. GARD lists these:
- Stiff legs
- Spastic walk
- Brisk reflexes
- High-arched feet (pes cavus)
- Mild intellectual disability
- Nerve damage affecting movement
Not everyone has every symptom. GARD's list comes from the Human Phenotype Ontology.
Diagnosis
- 1Talk with your doctor
Share the symptoms you've noticed, when they started and your family health history. Notes and photos can help.
- 2See a specialist
Specialists who may be involved include brain and nervous system specialists and genetic specialists.
- 3Ask which tests can help
Your care team will decide which exams and tests can confirm the diagnosis.
- 4Connect with expert centers
Spastic Paraplegia Foundation may keep lists of experts for this condition.
Care & treatment
- Care team
- Brain and nervous system specialists (neurologists); Genetic specialists (geneticists)
- Expert care
- Expert lists: Spastic Paraplegia Foundation
- Treatment
- GARD doesn't list specific treatments for this condition. Your care team will tailor care to your symptoms.
- Research
- Clinical trials and observational studies may be options. See the research section below.
General information, not medical advice. Your care team makes the decisions.
Everyday life
Living with a rare condition is easier with support.
- Connect with Spastic Paraplegia Foundation
- Keep notes on symptoms, changes and questions for appointments
- Ask about patient registries that help research
- Look into financial aid and travel resources for care visits
Quick facts
GARD links it to variation in chromosome region 3q27-q28 and doesn't name a gene. It is autosomal recessive, so a child inherits a changed copy of the gene from each parent.
Also known as: autosomal recessive spastic paraplegia 14; autosomal recessive spastic paraplegia type 14; hereditary spastic paraplegia type 14; spastic paraplegia 14; spastic paraplegia 14, autosomal recessive; spg14
Patient organizations
- Spastic Paraplegia FoundationHereditary spastic paraplegia · United States
Broader rare-disease groups
- Global GenesRare Diseases · United States
- National Organization for Rare DisordersRare Diseases · United States
- Genetic AllianceRare Diseases · United States
- RARE FoundationRare Diseases · United States
You are more than your diagnosis
Perspectives from people navigating life with Hereditary spastic paraplegia 14.
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