A multiple congenital anomalies (MCA) syndrome involving connective tissue characterized by growth retardation, alopecia, pseudoanodontia and ocular manifestations
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.
Actionable guidance for navigating care for GAPO syndrome
As GAPO syndrome is a rare condition with genetic implications, seeking a genetic counselor is crucial. You can find a genetic counselor at findageneticcounselor.com. Additionally, consider reaching out to specialists in congenital anomalies or genetic disorders, as they may provide valuable insights into managing the condition. While there are no identified patient organizations specific to GAPO syndrome, resources like GARD (rarediseases.info.nih.gov) and NORD (rarediseases.org) can offer support and information on rare diseases. If you are looking for specialized care, inquire about centers of excellence that focus on genetic syndromes or congenital anomalies, as they may have more experience with 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.
Online Mendelian Inheritance in Man
European rare disease database
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.
Organizations with orphan designations or approved therapies for this disease