A cataract that has material basis in variation in the region 1pter-p36.13.
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
The documentation surrounding cataract 8 multiple types is limited due to its rarity and the lack of systematic clinical studies. Conditions like this often affect fewer individuals, making it challenging for researchers to gather comprehensive data. Additionally, the genetic basis has not yet been identified, which complicates efforts to fully characterize the condition and its implications. However, ongoing research may provide new insights in the future.
The defining clinical feature of cataract 8 multiple types is the presence of nuclear cataracts, which are often evident from birth. These cataracts can lead to significant visual impairment if not addressed. As this condition primarily affects the lens of the eye, it is critical to monitor visual development, especially in pediatric patients. Regular ophthalmological evaluations are essential to assess the progression of cataracts and determine the need for surgical intervention.
To navigate cataract 8 multiple types, consider seeking a pediatric ophthalmologist with experience in congenital cataracts. They can provide specialized care and management options tailored to your child's needs. Additionally, genetic counseling may be beneficial, especially for family planning and understanding inheritance patterns. Resources such as the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide further information and support. While no patient organizations are currently identified, connecting with broader rare disease communities may offer valuable insights and support.
Currently, there is one active clinical trial related to cataract 8 multiple types. This trial may explore potential treatments or interventions for the condition. You can find more information and search for eligibility on ClinicalTrials.gov at the following link: https://clinicaltrials.gov/search?cond=cataract%208%20multiple%20types. Participation in clinical trials can offer hope for new therapies and a better understanding of the condition.
Actionable guidance for navigating care for cataract 8 multiple types
To navigate cataract 8 multiple types, consider seeking a pediatric ophthalmologist with experience in congenital cataracts. They can provide specialized care and management options tailored to your child's needs. Additionally, genetic counseling may be beneficial, especially for family planning and understanding inheritance patterns. Resources such as the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide further information and support. While no patient organizations are currently identified, connecting with broader rare disease communities may offer valuable insights and support.
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.
Age of onset indicates when symptoms typically first appear.
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
European rare disease database
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.