Hypermobile Ehlers-danlos Syndrome
What's New
Last Posted: Oct 01, 2024
- Low vitamin C status and hypermobility-related disorders in patients with bleeding disorder of unknown cause.
Eva Leinøe, et al. Haemophilia : the official journal of the World Federation of Hemophilia 2024 0 - Social media use by patients with hypermobile Ehlers-Danlos syndrome.
Colin M E Halverson et al. Mol Genet Genomic Med 2024 12(6) e2467 - Genetic complexity of diagnostically unresolved Ehlers-Danlos syndrome.
Anthony M Vandersteen, et al. Journal of medical genetics 2023 0 - High overlap in patients diagnosed with hypermobile Ehlers-Danlos syndrome or hypermobile spectrum disorders with fibromyalgia and 40 self-reported symptoms and comorbidities.
DeLisa Fairweather, et al. Frontiers in medicine 2023 0 1096180 - Hereditary alpha-tryptasemia modifies clinical phenotypes among individuals with congenital hypermobility disorders.
Vazquez Maribel, et al. HGG advances 2022 0 (2) 100094 - Pain Characteristics and Symptom Management in Children with Hypermobile Ehlers-Danlos Syndrome and Hypermobility Spectrum Disorder.
Jeong Hyo-Jung et al. Physical & occupational therapy in pediatrics 2023 1-14 - Assessment of the beliefs, needs, and expectations for genetic counseling of patients with hypermobile Ehlers-Danlos syndrome.
Ahimaz Priyanka et al. American journal of medical genetics. Part A 2022 188(11) 3172-3183 - Home-based exercise therapy for treating shoulder instability in patients with hypermobile Ehlers-Danlos syndrome/hypermobility spectrum disorders. A randomized trial.
Spanhove Valentien et al. Disability and rehabilitation 2022 1-11 - Patients with Ehlers-Danlos syndrome on the diagnostic odyssey: Rethinking complexity and difficulty as a hero's journey.
Halverson Colin Michael Egenberger et al. American journal of medical genetics. Part C, Seminars in medical genetics 2021 - Factors affecting quality of life in children and adolescents with hypermobile Ehlers-Danlos syndrome/hypermobility spectrum disorders.
Mu Weiyi et al. American journal of medical genetics. Part A 2019 Jan
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Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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