Familial chondromalacia patellae is an inherited bone disorder described in 5 families in 1963 and is characterized by localized patellar pain and male-to-male transmission.
Comprehensive, easy-to-understand information about this condition
How we create this content →Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 8, 2026
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 8, 2026
The limited documentation surrounding chondromalacia patellae is primarily due to its rarity, which restricts the ability to conduct extensive clinical studies. As this condition affects a small number of families, systematic collection of clinical data and phenotypic characterization has not yet been achieved. This can understandably lead to frustration for those affected, as comprehensive information and resources are scarce.
To navigate your care effectively, consider consulting with an orthopedic specialist who has experience in patellar disorders. They can provide tailored management strategies and help you understand your condition better. Additionally, the National Organization for Rare Disorders (NORD) offers resources and support for families dealing with rare conditions; you can find more information at rarediseases.org. Although no patient organizations are currently identified for chondromalacia patellae, participating in clinical trials may also provide access to cutting-edge research and treatment options.
Currently, there are three active clinical trials investigating chondromalacia patellae. These trials may explore various aspects of the condition, including potential treatments and management strategies. For more information on these studies, you can visit ClinicalTrials.gov and search for 'chondromalacia patellae'. This research represents a hopeful avenue for better understanding and managing the condition.
Actionable guidance for navigating care for chondromalacia patellae
To navigate your care effectively, consider consulting with an orthopedic specialist who has experience in patellar disorders. They can provide tailored management strategies and help you understand your condition better. Additionally, the National Organization for Rare Disorders (NORD) offers resources and support for families dealing with rare conditions; you can find more information at rarediseases.org. Although no patient organizations are currently identified for chondromalacia patellae, participating in clinical trials may also provide access to cutting-edge research and treatment options.
Consider asking your healthcare providers these condition-specific questions
Helpful links for rare disease information and support
Inheritance patterns describe how genetic conditions are passed from parents to children.
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 8, 2026
Consider asking your healthcare providers these condition-specific questions
Online Mendelian Inheritance in Man
European rare disease database
AI-Generated Content: This summary was generated using AI. Content has been fact-checked. Always consult with qualified healthcare providers for medical guidance.
Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.