10q22.3q23.3 microdeletion syndrome is a rare partial autosomal monosomy characterized by a mild facial dysmorphism variably including macrocephaly, broad forehead, hypertelorism or hypotelorism, deep...
Comprehensive, easy-to-understand information about this condition
How we create this content →Documentation for chromosome 10q23 deletion syndrome is limited primarily due to its rarity, which restricts the scope of systematic clinical studies. The lack of identified genes and established inheritance patterns further complicates the characterization of this condition. As research continues, there is hope that more information will be gathered to better understand and manage this syndrome.
To find the best care for chromosome 10q23 deletion syndrome, consider consulting a geneticist who specializes in rare genetic disorders. They can provide insights into genetic counseling and potential testing for family members. While there are currently no specific patient organizations or registries for this condition, organizations like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide valuable resources and support. Engaging with healthcare providers who have experience in managing similar syndromes will also be beneficial.
Actionable guidance for navigating care for chromosome 10q23 deletion syndrome
To find the best care for chromosome 10q23 deletion syndrome, consider consulting a geneticist who specializes in rare genetic disorders. They can provide insights into genetic counseling and potential testing for family members. While there are currently no specific patient organizations or registries for this condition, organizations like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide valuable resources and support. Engaging with healthcare providers who have experience in managing similar syndromes will also be beneficial.
Consider asking your healthcare providers these condition-specific questions
Helpful links for rare disease information and support
Documentation for chromosome 10q23 deletion syndrome is limited primarily due to its rarity, which restricts the scope of systematic clinical studies. The lack of identified genes and established inheritance patterns further complicates the characterization of this condition. As research continues, there is hope that more information will be gathered to better understand and manage this syndrome.
To find the best care for chromosome 10q23 deletion syndrome, consider consulting a geneticist who specializes in rare genetic disorders. They can provide insights into genetic counseling and potential testing for family members. While there are currently no specific patient organizations or registries for this condition, organizations like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide valuable resources and support. Engaging with healthcare providers who have experience in managing similar syndromes will also be beneficial.
Actionable guidance for navigating care for chromosome 10q23 deletion syndrome
To find the best care for chromosome 10q23 deletion syndrome, consider consulting a geneticist who specializes in rare genetic disorders. They can provide insights into genetic counseling and potential testing for family members. While there are currently no specific patient organizations or registries for this condition, organizations like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide valuable resources and support. Engaging with healthcare providers who have experience in managing similar syndromes will also be beneficial.
Consider asking your healthcare providers these condition-specific questions
Helpful links for rare disease information and support
Documentation for chromosome 10q23 deletion syndrome is limited primarily due to its rarity, which restricts the scope of systematic clinical studies. The lack of identified genes and established inheritance patterns further complicates the characterization of this condition. As research continues, there is hope that more information will be gathered to better understand and manage this syndrome.
To find the best care for chromosome 10q23 deletion syndrome, consider consulting a geneticist who specializes in rare genetic disorders. They can provide insights into genetic counseling and potential testing for family members. While there are currently no specific patient organizations or registries for this condition, organizations like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide valuable resources and support. Engaging with healthcare providers who have experience in managing similar syndromes will also be beneficial.
Actionable guidance for navigating care for chromosome 10q23 deletion syndrome
To find the best care for chromosome 10q23 deletion syndrome, consider consulting a geneticist who specializes in rare genetic disorders. They can provide insights into genetic counseling and potential testing for family members. While there are currently no specific patient organizations or registries for this condition, organizations like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide valuable resources and support. Engaging with healthcare providers who have experience in managing similar syndromes will also be beneficial.
Consider asking your healthcare providers these condition-specific questions
Helpful links for rare disease information and support
Age of onset indicates when symptoms typically first appear.
Consider asking your healthcare providers these condition-specific questions
Online Mendelian Inheritance in Man
European rare disease database
Genetic and Rare Diseases Info Center
AI-Generated Content: This summary was generated using AI. Content has been fact-checked. Always consult with qualified healthcare providers for medical guidance.
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