Hypermobile Ehlers-Danlos Syndrome (hEDS) is one of 13 recognised subtypes of
inherited connective tissue disorders known as Ehlers-Danlos syndrome. It is the
most common form, accounting for 80-90% of cases. The disease is estimated to
affect 1 in 5000 people, with a gender ratio of 10 women to 1 man. This paper aims
to evaluate the symptoms and manifestations of hEDS in women and to identify the
factors that lead to delayed or missed diagnosis. The higher prevalence of hEDS in
women, the observed later diagnosis in girls during childhood, and the significant
negative consequences of diagnostic delays require a greater focus on earlier
diagnosis and proper management. Greater educational efforts directed at clinicians
are needed to ensure timely identification and appropriate care for women with
hEDS.
Keywords: hEDS, hypermobile Ehlers-Danlos Syndrome, women, hypermobility