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(e.g., a defect in lysine-hydroxylysine cross-linking of tropocollagen leads to unstable collagen fibrils or procollagen peptidase deficiency ) [3] Autosomal dominant or recessive inheritance with varying patterns of inheritance, severity, and type of collagen affected Ehlers-Danlos syndrome is subclassified into 13 different types, based on clinical presentation, genetic defect, and type of collagen affected (e.g., hypermobility type, classical type)

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