A cataract that has material basis in mutation in the region 14q22-q23.
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 7, 2026
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 7, 2026
Documentation on cataract 32 multiple types is limited due to its rarity and the lack of systematic studies. As this condition affects a small number of individuals, comprehensive clinical characterization and research have been challenging. The genetic basis has not yet been identified, which further complicates efforts to understand the condition fully.
To navigate cataract 32 multiple types, consider consulting with an ophthalmologist who has expertise in genetic eye disorders. They can provide insights into management strategies and potential interventions. Additionally, you can explore resources like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov for more information. While there are no identified patient organizations, staying connected with genetic counseling services may provide support for you and your family regarding inheritance patterns and family planning.
Currently, there is one active clinical trial related to cataract 32 multiple types. You can explore participation opportunities and details about the trial by visiting ClinicalTrials.gov and searching for 'cataract 32 multiple types'. While there are no orphan drugs designated for this condition, the ongoing research may provide insights into potential future treatments.
Actionable guidance for navigating care for cataract 32 multiple types
To navigate cataract 32 multiple types, consider consulting with an ophthalmologist who has expertise in genetic eye disorders. They can provide insights into management strategies and potential interventions. Additionally, you can explore resources like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov for more information. While there are no identified patient organizations, staying connected with genetic counseling services may provide support for you and your family regarding inheritance patterns and family planning.
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 7, 2026
Consider asking your healthcare providers these condition-specific questions
Online Mendelian Inheritance in Man
AI-Generated Content: This summary was generated using AI. 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.