Coexistence of spinocerebellar ataxia autosomal recessive type 21 and Ehlers-Danlos syndrome spondylodysplastic type 3 in a patient

MeSH terms

• Ehlers-Danlos Syndrome* / complications
• Ehlers-Danlos Syndrome* / diagnosis
• Ehlers-Danlos Syndrome* / genetics
• Humans
• Inheritance Patterns
• Spinocerebellar Ataxias* / complications
• Spinocerebellar Ataxias* / diagnosis
• Spinocerebellar Ataxias* / genetics