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 limited documentation regarding arthrogryposis, distal, IIa 11 can be attributed to its rarity, with few cases reported globally. This extreme rarity restricts the ability to conduct extensive clinical studies, leading to gaps in understanding the full spectrum of the condition. Additionally, the genetic basis was only recently identified, and ongoing clinical characterization is necessary to provide more comprehensive insights.
The key clinical features of arthrogryposis, distal, IIa 11 primarily affect the hands and forearms. Camptodactyly is consistently present, leading to a characteristic bending of the fingers. Additionally, many individuals exhibit absent proximal finger flexion creases, which may impact hand function. Limited movement in the forearm can also affect daily activities. These features highlight the importance of early intervention and tailored support.
To manage arthrogryposis, distal, IIa 11, consider consulting a geneticist who specializes in hereditary conditions, as they can provide valuable insights into genetic testing and family planning. While there are no identified patient organizations, resources such as the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov may offer useful information. Genetic counseling is recommended for understanding the implications of the MET gene variant in your family. Additionally, inquire about any natural history studies that may be relevant to your condition.
Actionable guidance for navigating care for arthrogryposis, distal, IIa 11
To manage arthrogryposis, distal, IIa 11, consider consulting a geneticist who specializes in hereditary conditions, as they can provide valuable insights into genetic testing and family planning. While there are no identified patient organizations, resources such as the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov may offer useful information. Genetic counseling is recommended for understanding the implications of the MET gene variant in your family. Additionally, inquire about any natural history studies that may be relevant to your 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
AI-Generated Content: This summary was generated using AI. Always consult with qualified healthcare providers for medical guidance.
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