PurposeEhlers-Danlos syndrome type IV (EDS-IV) results from abnormal procollagen III synthesis and leads to arterial, intestinal, and uterine rupture. The purpose of this study was to review the spectrum, management, and clinical outcome of EDS-IV patients.MethodsWe retrospectively reviewed the clinical data of 31 patients (15 male and 16 female) with a clinical diagnosis of EDS-IV treated over a 30-year period (1971 to 2001). Biochemical confirmation was obtained in 24 patients, and mutation of the COL3A1 gene was confirmed in 11 patients. The study excluded patients with other connective tissue dysplasias.ResultsThe mean age at the time of diagnosis was 28.5 ± 11 years (range, 10 to 53 years). Twenty-four patients developed 132 vascular c...
SummaryEhlers–Danlos syndrome (EDS) is a group of well described connective tissue disorders in whic...
AbstractA 61-year-old man presented with an acute type B aortic dissection for which a stent-graft w...
Ehlers-Danlos syndrome (EDS) is a rare disorder that occurs due to genetic defect in the collagen sy...
ObjectivesThere has been debate regarding the safety of performing elective procedures in patients w...
Ehlers-Danlos syndrome is the most common inherited connective tissue disease and is a consequence o...
Ehlers-Danlos type IV (EDS-IV) is an inherited condition most notable for its associated vascular co...
BACKGROUND Ehlers-Danlos syndrome (EDS) is a heterogeneous group of rare inherited disease...
Purpose: Within the spectrum of the Ehlers-Danlos syndromes (EDS), vascular complications are usuall...
AbstractEhlers-Danlos syndrome type IV (EDS type IV), the vascular type, results from mutations in t...
AbstractEhlers-Danlos syndrome type IV is the most lethal variant of that illness and is associated ...
AbstractEhlers–Danlos syndrome (EDS) is a hereditary disorder of the connective tissue. Ten differen...
Ehlers-Danlos syndrome is a rare inherited disease of connective tissue. Patients with type IV Ehler...
BACKGROUND Ehlers-Danlos syndrome (EDS) is a heterogeneous group of rare inherited diseas...
AbstractArterial complications in Ehlers-Danlos Syndrome (EDS) are rare and may be life-threatening....
Ehlers-Danlos syndrome (EDS) represents a group of inheritable connective tissue disorders. Patients...
SummaryEhlers–Danlos syndrome (EDS) is a group of well described connective tissue disorders in whic...
AbstractA 61-year-old man presented with an acute type B aortic dissection for which a stent-graft w...
Ehlers-Danlos syndrome (EDS) is a rare disorder that occurs due to genetic defect in the collagen sy...
ObjectivesThere has been debate regarding the safety of performing elective procedures in patients w...
Ehlers-Danlos syndrome is the most common inherited connective tissue disease and is a consequence o...
Ehlers-Danlos type IV (EDS-IV) is an inherited condition most notable for its associated vascular co...
BACKGROUND Ehlers-Danlos syndrome (EDS) is a heterogeneous group of rare inherited disease...
Purpose: Within the spectrum of the Ehlers-Danlos syndromes (EDS), vascular complications are usuall...
AbstractEhlers-Danlos syndrome type IV (EDS type IV), the vascular type, results from mutations in t...
AbstractEhlers-Danlos syndrome type IV is the most lethal variant of that illness and is associated ...
AbstractEhlers–Danlos syndrome (EDS) is a hereditary disorder of the connective tissue. Ten differen...
Ehlers-Danlos syndrome is a rare inherited disease of connective tissue. Patients with type IV Ehler...
BACKGROUND Ehlers-Danlos syndrome (EDS) is a heterogeneous group of rare inherited diseas...
AbstractArterial complications in Ehlers-Danlos Syndrome (EDS) are rare and may be life-threatening....
Ehlers-Danlos syndrome (EDS) represents a group of inheritable connective tissue disorders. Patients...
SummaryEhlers–Danlos syndrome (EDS) is a group of well described connective tissue disorders in whic...
AbstractA 61-year-old man presented with an acute type B aortic dissection for which a stent-graft w...
Ehlers-Danlos syndrome (EDS) is a rare disorder that occurs due to genetic defect in the collagen sy...