Results 41 to 50 of about 1,247,077 (145)

Supplemental Material - Agreement between parent-proxy and child self-report in pediatric hypermobile Ehlers-Danlos syndrome

, 2022
Supplemental Material for Agreement between parent-proxy and child self-report in pediatric hypermobile Ehlers-Danlos syndrome by Michael Muriello, You Wang, Julia L Clemens, Weiyi Mu, Christy H Smith, Phuong T Tran, Peter C Rowe, Clair Francomano ...
Michael Muriello (13843006), Julia L Clemens (13843003), You Wang (312086), Phuong T Tran (13843015), Weiyi Mu (13843009), Joann Bodurtha (9170451), Clair Francomano (13843021), Christy H Smith (13843012), Antonie D Kline (13843024), Peter C Rowe (13843018)   +9 more
core   +1 more source

Physical and mechanical therapies for lower limb symptoms in children with Hypermobility Spectrum Disorder and Hypermobile Ehlers-Danlos Syndrome: a systematic review

Journal of Foot and Ankle Research, 2018
Background Hypermobility Spectrum Disorder and Hypermobile Ehlers Danlos Syndrome are two common heritable genetic disorders of connective tissue. Both conditions are characterised by excessive joint range of motion and the presence of musculoskeletal ...
Benjamin Peterson, Andrea Coda, Verity Pacey, Fiona Hawke   +3 more
doaj   +1 more source

Supplemental Material - The role of functional disability and social support in psychological outcomes for individuals with pediatric hypermobile ehlers–danlos syndrome

, 2022
Supplemental Material for The role of functional disability and social support in psychological outcomes for individuals with pediatric hypermobile ehlers–danlos syndrome by Keely H Bieniak, Brad T Tinkle, Susan T Tran in Journal of Child Health ...
Brad T Tinkle (14242514), Keely H Bieniak (14242511), Susan T Tran (14242517)   +2 more
core   +1 more source

Pediatric joint hypermobility: a diagnostic framework and narrative review

Orphanet Journal of Rare Diseases, 2023
Background Hypermobile Ehlers–Danlos syndrome (hEDS) and hypermobility spectrum disorders (HSD) are debilitating conditions. Diagnosis is currently clinical in the absence of biomarkers, and criteria developed for adults are difficult to use in children ...
Louise Jane Tofts, Jane Simmonds, Sarah B. Schwartz, Roberto M. Richheimer, Constance O’Connor, Ellen Elias, Raoul Engelbert, Katie Cleary, Brad T. Tinkle, Antonie D. Kline, Alan J. Hakim, Marion A. J. van Rossum, Verity Pacey   +12 more
doaj   +1 more source

Desmoid Fibromatosis Presenting with Gastrointestinal Manifestations in a Patient with Ehlers-Danlos Syndrome: A Case Report [PDF]

Journal of Clinical and Diagnostic Research
Ehlers-Danlos syndrome comprises 13 hereditary connective tissue disorders associated with skin hyperelasticity, joint hypermobility, atrophic scarring, and blood vessel fragility.
Elias Lugo-Fagundo, Edmund M Weisberg, Ryan C Rizk, Elliot K Fishman   +3 more
doaj   +1 more source

Síndroma de Ehlers-Danlos – Uma causa rara de pneumotórax espontâneo

Revista Portuguesa de Pneumologia, 2006
Resumo: A síndroma de Ehlers-Danlos (cutis hyperelastica), constitui uma patologia do tecido conjuntivo caracterizada por alterações da pele, ligamentos e órgãos internos.Apresenta transmissão hereditária, em geral autossómica dominante.
Carlos Lopes, Alda Manique, Renato Sotto-Mayor, Jorge Cruz, Margarida Mendes de Almeida, João Cravino, A Bugalho de Almeida   +6 more
doaj   +1 more source

Clinician-associated traumatization from difficult medical encounters: Results from a qualitative interview study on the Ehlers-Danlos Syndromes

SSM: Qualitative Research in Health, 2023
Patients with hypermobile Ehlers Danlos Syndrome often experience psychological distress resulting from the perceived hostility and disinterest of their clinicians.
Colin M.E. Halverson, Heather L. Penwell, Clair A. Francomano   +2 more
doaj   +1 more source

Hypoglycemia Associated With Hypermobile Ehlers-Danlos Syndrome

JCEM Case Reports
Abstract Hypoglycemia in the absence of diabetes is often multifactorial and challenging to diagnose definitively. We present a case report and an expanded series of adult females with reactive hypoglycemia who were diagnosed with Ehlers-Danlos syndrome (EDS).
Hamayle Saeed, Amanda Sheehan, Mary-Elizabeth Patti   +2 more
openaire   +2 more sources

Cardiovascular autonomic dysfunction in Ehlers–Danlos syndrome—Hypermobile type [PDF]

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2017
Autonomic dysfunction contributes to health‐related impairment of quality of life in the hypermobile type of Ehlers–Danlos syndrome (hEDS). Typical signs and symptoms include tachycardia, hypotension, gastrointestinal dysmotility, and disturbed bladder function and sweating regulation.
Alan, Hakim, Chris, O'Callaghan, Inge, De Wandele, Lauren, Stiles, Alan, Pocinki, Peter, Rowe   +5 more
openaire   +2 more sources

The association between collagenopathies and the risk of spontaneous preterm birth: A systematic review with selective meta‐analysis

Acta Obstetricia et Gynecologica Scandinavica, EarlyView.
This review quantifies the association between collagenopathies and spontaneous preterm birth, assessing their role in antenatal risk assessment. Marfan syndrome is significantly associated with an increased risk of spontaneous preterm birth (OR 2.71, 95% CI 2.23–3.30; p < 0.001; I2 = 41%) while evidence for Ehlers–Danlos syndrome is heterogeneous ...
Kensie Treacy, Brenda F. Narice, Denya Williams‐Goss, Dilly O. C. Anumba   +3 more
wiley   +1 more source