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Related to Ehlers-Danlos syndrome: Marfan syndrome
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References in periodicals archive ?
Pepin M, Schwarzer U, Superto A, Byers PH (2000) Clinical and genetic features of Ehlers-Danlos syndrome type IV, the vascular type.
Rombaut L, Malfait F Cools A, De Paepe A, Calders P Musculoskeletal complaints, physical activity and health-related quality of life among patients with the Ehlers-Danlos syndrome hypermobility type.
Proceeds from the funding round will primarily be used to prepare a new drug application (NDA) for ACER-002 (celiprolol hydrochloride), Acer's lead candidate which is being developed for the treatment of vascular Ehlers-Danlos Syndrome (vEDS), a rare, life-threatening genetic connective tissue disorder.
Multiple supernumerary teeth (MSNT) and Ehlers-Danlos syndrome (EDS): a case report.
Eckardt, "Spontaneous gluteal artery rupture resulting in compartment syndrome and sciatic neuropathy: report of a case in Ehlers-Danlos syndrome," Clinical Orthopaedics and Related Research, no.
She was diagnosed with Ehlers-Danlos syndrome in her late 30's; prior to that, she had been living with her worsening symptoms, unaware of her diagnosis.
In fact, the Rubery 34-yearold was suffering from the rare condition Ehlers-Danlos Syndrome (EDS).
Heritable connective tissue disorders such as type IV Ehlers-Danlos syndrome, Marfan syndrome, and type I osteogenesis imperfecta predispose patients to dissection.
Turner who has appeared on TV shows such as Britain's Got Talent has developed his extreme case of Ehlers-Danlos syndrome - a rare genetic skin condition into an extraordinary talent, plying his skin in ways never thought possible.
We meet some of the kids staying at the Royal Manchester Children's Hospital, including Emily, 15, who has a rare genetic condition called Ehlers-Danlos syndrome.
Tim Tebow has fulfilled the dream of Haley Burke, a girl who was diagnosed with life-threatening illness Ehlers-Danlos Syndrome at an early of 15 years old.
George resident who was diagnosed with Ehlers-Danlos syndrome (EDS).
NYSE MKT: FCSC) and Intrexon Corporation (XON) will expand their exclusive channel collaboration to develop a treatment for Ehlers-Danlos syndrome hypermobility type (EDS-HT), a rare genetic disorder resulting in weakened connective tissue.
This year they were Skanda Vale Hospice; the Rudy Trust; the Ehlers-Danlos Syndrome (EDS) charity and the District Brownies Centenary Appeal.
4 Joint hypermobility is a very common finding in conditions of known connective tissue abnormalities, such as the Ehlers-Danlos syndrome, and is considered a reliable marker for altered connective tissue.