Non-syndromic limb reduction defect
MONDO:0019713Also known as: non-syndromic limb hypoplasia, nonsyndromic limb reduction defect, isolated limb reduction defect
35 clinical trials for this condition and its sub-types, 0 tagged with Non-syndromic limb reduction defect itself.
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Sub-types of Non-syndromic limb reduction defect
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Clubfoot 18 trials
2 sub-types
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Non-syndromic amelia 1 trial · 5 incl. sub-types
3 sub-types
- Amelia of lower limb 2 trials Sub-types →
- Amelia of upper limb 2 trials Sub-types →
- Tetra-amelia 0 trials
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Poland syndrome 2 trials
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Hemimelia 0 trials · 2 incl. sub-types
5 sub-types
- Radial hemimelia 0 trials · 1 incl. sub-types Sub-types →
- Ulnar hemimelia 1 trial Sub-types →
- Complete hemimelia 0 trials
- Fibular hemimelia 0 trials Sub-types →
- Tibial hemimelia 0 trials Sub-types →
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Cornelia de Lange syndrome 1 1 trial
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Duane-radial ray syndrome 1 trial
2 sub-types
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Femoral agenesis/hypoplasia 1 trial
2 sub-types
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Femur-fibula-ulna complex 1 trial
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Adams-Oliver syndrome 1 0 trials
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Adams-Oliver syndrome 2 0 trials
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Adams-Oliver syndrome 3 0 trials
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Adams-Oliver syndrome 4 0 trials
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Adams-Oliver syndrome 5 0 trials
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Adams-Oliver syndrome 6 0 trials
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Cornelia de Lange syndrome 2 0 trials
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Cornelia de Lange syndrome 3 0 trials
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Cornelia de Lange syndrome 4 0 trials
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Cornelia de Lange syndrome 5 0 trials
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Fuhrmann syndrome 0 trials
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Gollop-Wolfgang complex 0 trials
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Holt-Oram syndrome 0 trials
1 sub-type
- Heart-hand syndrome type 3 0 trials
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Hypoglossia-hypodactyly syndrome 0 trials
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Roberts-SC phocomelia syndrome 0 trials
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Acheiropody 0 trials
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Adactylia, unilateral 0 trials
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Femoral-facial syndrome 0 trials
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Humeral agenesis/hypoplasia 0 trials
2 sub-types
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Pelvis-shoulder dysplasia 0 trials
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Pelviscapular dysplasia 0 trials
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Phocomelia, Schinzel type 0 trials
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Rapadilino syndrome 0 trials
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Tetraamelia syndrome 1 0 trials
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Tetraamelia syndrome 2 0 trials
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Thrombocythemia 1 0 trials
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Ulnar-mammary syndrome 0 trials
Most studied deeper sub-types
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Gene therapy for rare blood disease passes 15-Year safety watch
Disease control OngoingThis study follows 9 people with Fanconi Anemia who already received a gene therapy that adds a working FANCA gene to their blood stem cells. Researchers will check their health and blood counts for 15 years to see if the treatment remains safe and keeps working. No new treatment…
Sponsor: Rocket Pharmaceuticals Inc. • Aim: Disease control
Last updated Jun 27, 2026 12:07 UTC
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Experimental gene therapy aims to stop bone marrow failure in kids with rare disease
Disease control OngoingThis phase 2 trial tests a gene therapy called RP-L102 for children with Fanconi anemia subtype A, a rare genetic disorder that leads to bone marrow failure. Doctors take the child's own blood stem cells, fix the faulty gene in a lab, and infuse the corrected cells back. The goal…
Phase 2 • Sponsor: Rocket Pharmaceuticals Inc. • Aim: Disease control
Last updated Jun 27, 2026 08:06 UTC
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New scoring tool aims to predict clubfoot recurrence in kids
Knowledge-focused OngoingThis study follows 60 children aged 4–10 with clubfoot to see if a new scoring system (PBS-score) can predict whether their foot condition will come back and need extra treatment like casting, braces, or surgery. Researchers will track the children for five years and also ask fam…
Sponsor: Region Stockholm • Aim: Knowledge-focused
Last updated Jun 26, 2026 17:07 UTC