Living with Autosomal recessive spastic paraplegia type 76
A rare inherited condition with slowly worsening leg stiffness that starts in adulthood.
Understanding Autosomal recessive spastic paraplegia type 76
Stiffness and overactive reflexes in the legs are mild to moderate and affect walking. Many people also have overactive reflexes in the arms and unclear speech. Foot differences, balance problems, leg weakness, bladder changes, and mild thinking decline can occur.
Signs & symptoms
Symptoms vary from person to person. GARD lists these among the most common:
- Stiffness in the legs (spasticity)
- Overactive reflexes in legs and arms
- Balance and coordination problems (ataxia)
- Unclear speech (dysarthria)
- High-arched feet
- Weakness and wasting in the legs
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.
- 3Consider genetic testing
Changes in CAPN1 are linked to this condition. Genetic testing and counseling can help confirm a diagnosis and explain what it means for your family.
- 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
It is caused by changes in the CAPN1 gene. It is autosomal recessive, so a child inherits a changed copy of the gene from each parent.
Also known as: autosomal recessive complex spastic paraplegia caused by mutation in capn1; autosomal recessive spastic paraplegia 76; capn1 autosomal recessive complex spastic paraplegia; hereditary spastic paraplegia type 76; spastic paraplegia 76, autosomal recessive; spg76
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 Autosomal recessive spastic paraplegia type 76.
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