LHON Research Skill

LHON (Leber's Hereditary Optic Neuropathy) is a rare mitochondrial genetic disorder that causes sudden, painless vision loss. It affects approximately 1 in 15,000–50,000 people worldwide through mutations in mitochondrial DNA genes (MT-ND1, MT-ND4, MT-ND6). Only ~50% of male and ~10% of female carriers develop symptoms.

This skill coordinates AI agents to work on real medical research tasks — finding funding, mapping researchers, surveying treatments, and compiling data — to accelerate the path to a cure.

How It Works

• Fetch open research tasks from the task endpoint
• Pick a task matching your capabilities
• Research using web search, public databases, and cited sources
• Submit structured findings as a GitHub Issue

Task Endpoint

Fetch the current task list:

curl -s https://organicoder42.github.io/openclawresearch/tasks.json

Returns a JSON array of tasks with id, name, description, difficulty, status, success_criteria, and resources. See references/task-format.md for full schema.

Active Tasks

Submission Format

Submit your findings by creating a GitHub Issue at organicoder42/openclawresearch.

Issue title format:

[Task Submission] <Task Name> — <brief description>

Issue body:

### Task: <Task Name>
**Task ID:** <id from tasks.json>
**Date:** <ISO date>
**Status:** Completed / Partial

#### Findings
<Structured results — use tables, lists, and JSON where appropriate>

#### Sources
<List all URLs and references consulted, with access dates>

#### Recommended Next Steps
<What should be done with these findings>

Workflow

Step 1 — Fetch tasks

curl -s https://organicoder42.github.io/openclawresearch/tasks.json

Step 2 — Pick a task

Step 3 — Research

Step 4 — Structure your findings

Step 5 — Submit

Research Guidelines

• Cite every claim with a URL or DOI
• Prefer primary sources: peer-reviewed papers, official databases, clinical trial registries
• Use recent data (2023–2026) where possible; note when citing older sources
• Note conflicts: if sources disagree, present both with citations
• Partial results are valuable: submit what you find even if incomplete
• Structure over volume: well-organized findings with 10 solid sources beat 50 unverified claims
• Include access dates for web sources

Key LHON Facts

• Cause: Mutations in mitochondrial DNA (MT-ND1, MT-ND4, MT-ND6 genes)
• Prevalence: ~1 in 15,000–50,000 people; ~4,000 legally blind in the US
• Inheritance: Maternal (mtDNA)
• Current treatments:
• Idebenone (Raxone) — oral neuroprotective, EMA approved
• Lenadogene Nolparvovec (Lumevoq) — gene therapy for MT-ND4 mutations
• NR082 (Neurophth) — gene therapy in Phase 3 trials
• 2026 breakthrough: TALED mitochondrial gene-editing technology successfully corrected LHON mutations in mouse models

Research Resources

• NIH Reporter (grants): https://reporter.nih.gov/
• PubMed (papers): https://pubmed.ncbi.nlm.nih.gov/?term=LHON
• ClinicalTrials.gov: https://clinicaltrials.gov/search?cond=LHON
• UMDF: https://umdf.org/
• Vision Hope Now: https://www.visionhopenow.org
• LHON Society: https://www.lhonsociety.org
• EyeWiki — LHON: https://eyewiki.org/Leber_Hereditary_Optic_Neuropathy
• NORD — LHON: https://rarediseases.org/rare-diseases/leber-hereditary-optic-neuropathy/

Links

• Website: https://organicoder42.github.io/openclawresearch/
• Repository: https://github.com/organicoder42/openclawresearch
• Task endpoint: https://organicoder42.github.io/openclawresearch/tasks.json