Disorders of cornification that are characterized by visible scaling and/or hyperkeratosis of most or all of the skin. Inherited ichthyoses, defined as the generalized form of Mendelian disorders of c...
Comprehensive, easy-to-understand information about this condition
How we create this content →Patient Advocacy Groups (PAGs) provide support, resources, and community for patients and caregivers.
Consider asking your healthcare providers these condition-specific questions
European rare disease database
Genetic and Rare Diseases Info Center
Patient Advocacy Groups (PAGs) provide support, resources, and community for patients and caregivers.
Consider asking your healthcare providers these condition-specific questions
European rare disease database
Genetic and Rare Diseases Info Center
The limited documentation surrounding ichthyosis is primarily due to its heterogeneity and the rarity of specific forms. Many cases have not been systematically studied, and the genetic factors contributing to the condition are still being identified. This complexity can lead to frustration for patients seeking clarity and support.
To navigate your journey with ichthyosis, consider consulting a dermatologist with expertise in skin disorders, particularly those specializing in cornification disorders. The Foundation For Ichthyosis & Related Skin Types offers valuable resources and support for affected individuals and families. Additionally, you may want to explore participation in clinical trials, which can provide access to new treatments and contribute to research. For more information, visit their website at https://www.firstskinfoundation.org.
Currently, there are 33 active clinical trials related to ichthyosis, which may explore various treatment options and management strategies. Although no orphan drugs have been designated, the existence of these trials highlights ongoing research efforts aimed at understanding and treating this condition. For more details, you can explore the trials at ClinicalTrials.gov: https://clinicaltrials.gov/search?cond=ichthyosis.
Actionable guidance for navigating care for ichthyosis
To navigate your journey with ichthyosis, consider consulting a dermatologist with expertise in skin disorders, particularly those specializing in cornification disorders. The Foundation For Ichthyosis & Related Skin Types offers valuable resources and support for affected individuals and families. Additionally, you may want to explore participation in clinical trials, which can provide access to new treatments and contribute to research. For more information, visit their website at https://www.firstskinfoundation.org.
Consider asking your healthcare providers these condition-specific questions
Connect with organizations supporting the ichthyosis community
Helpful links for rare disease information and support
Clinical profile data for this condition is not yet available. Phenotype information may still be loading below.
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Feb 8, 2026
Patient Advocacy Groups (PAGs) provide support, resources, and community for patients and caregivers.
Consider asking your healthcare providers these condition-specific questions
European rare disease database
Genetic and Rare Diseases Info Center
1 peer-reviewed source from PubMed
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.