Case study highlights delayed diagnosis of Ehlers-Danlos syndrome, emphasizing public health implications.
Ehlers-Danlos Syndrome (EDS) is a rare, inherited connective tissue disorder, frequently diagnosed with significant delay due to fragmented care and lack of coordination among specialists. We present the case of a 35-year-old woman whose EDS diagnosis was established 17 years after the onset of symptoms. Despite numerous specia
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Agata Kulkowska- Gaj (2025) studied this question.
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