Any autosomal dominant nocturnal frontal lobe epilepsy in which the cause of the disease is a mutation in the CHRNB2 gene.
Comprehensive, easy-to-understand information about this condition
How we create this content →Inheritance patterns describe how genetic conditions are passed from parents to children.
Inheritance patterns describe how genetic conditions are passed from parents to children.
The documentation surrounding autosomal dominant nocturnal frontal lobe epilepsy 3 is limited due to its rarity and the recent identification of its genetic basis. As this condition affects a small number of individuals, comprehensive clinical studies have not been extensively conducted. This results in a lack of systematic documentation of clinical features and treatment options.
To navigate your care for autosomal dominant nocturnal frontal lobe epilepsy 3, consider consulting a neurologist who specializes in epilepsy, particularly one with experience in genetic forms of epilepsy. While there are currently no identified patient organizations, resources such as the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide additional information and support. Genetic counseling may also be beneficial for understanding the implications of the CHRNB2 mutation for you and your family. Unfortunately, there are no registries or natural history studies currently available for this condition.
Actionable guidance for navigating care for autosomal dominant nocturnal frontal lobe epilepsy 3
To navigate your care for autosomal dominant nocturnal frontal lobe epilepsy 3, consider consulting a neurologist who specializes in epilepsy, particularly one with experience in genetic forms of epilepsy. While there are currently no identified patient organizations, resources such as the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide additional information and support. Genetic counseling may also be beneficial for understanding the implications of the CHRNB2 mutation for you and your family. Unfortunately, there are no registries or natural history studies currently available for this condition.
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.
Consider asking your healthcare providers these condition-specific questions
Online Mendelian Inheritance in Man
Genetic and Rare Diseases Info Center
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.