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Pregnancy Outcome in Joint Hypermobility Syndrome and Ehlers–Danlos Syndrome
IntroductionAn increased risk of preterm birth in women with joint hypermobility syndrome or Ehlers-Danlos syndrome is suspected. Material and methodsIn this nationwide cohort study from 1997 through 2011, women with either joint hypermobility syndrome ...
Kari Johansson +2 more
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BMJ, 2010
Chronic pain, frequent soft tissue trauma, and exhaustion compelled a keen recreational ballet dancer to give up classes and ...
Isobel, Knight, H A, Bird
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Chronic pain, frequent soft tissue trauma, and exhaustion compelled a keen recreational ballet dancer to give up classes and ...
Isobel, Knight, H A, Bird
openaire +2 more sources
Current Opinion in Rheumatology, 1996
Inherited connective tissue disorders, among them Ehlers-Danlos syndrome, osteogenesis imperfecta, Marfan syndrome, and Larsen syndrome, are characterized by generalized joint hypermobility. Others, such as Morquio syndrome or achondroplasia, have hypermobility in a more limited distribution.
M L, Raff, P H, Byers
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Inherited connective tissue disorders, among them Ehlers-Danlos syndrome, osteogenesis imperfecta, Marfan syndrome, and Larsen syndrome, are characterized by generalized joint hypermobility. Others, such as Morquio syndrome or achondroplasia, have hypermobility in a more limited distribution.
M L, Raff, P H, Byers
openaire +2 more sources
BMJ, 2011
Joint hypermobility syndrome (JHS), previously known as benign joint hypermobility syndrome (BJHS), is a heritable disorder of connective tissue that comprises symptomatic hypermobility predisposing to arthralgia, soft tissue injury, and joint instability.1 It is indistinguishable from the hypermobility type of Ehlers-Danlos syndrome.2 Complications ...
Juliette, Ross, Rodney, Grahame
openaire +2 more sources
Joint hypermobility syndrome (JHS), previously known as benign joint hypermobility syndrome (BJHS), is a heritable disorder of connective tissue that comprises symptomatic hypermobility predisposing to arthralgia, soft tissue injury, and joint instability.1 It is indistinguishable from the hypermobility type of Ehlers-Danlos syndrome.2 Complications ...
Juliette, Ross, Rodney, Grahame
openaire +2 more sources
Rheumatic Disease Clinics of North America, 2013
Although perceived as a rare condition, joint hypermobility syndrome is common. Its prevalence in rheumatology clinics is extremely high. Early estimates suggest that it may be the most common of all rheumatologic conditions. The problem lies in the general lack of awareness of the syndrome, its means of recognition, and the resultant failure to ...
Asma, Fikree +2 more
openaire +2 more sources
Although perceived as a rare condition, joint hypermobility syndrome is common. Its prevalence in rheumatology clinics is extremely high. Early estimates suggest that it may be the most common of all rheumatologic conditions. The problem lies in the general lack of awareness of the syndrome, its means of recognition, and the resultant failure to ...
Asma, Fikree +2 more
openaire +2 more sources
Dysautonomia in the joint hypermobility syndrome
The American Journal of Medicine, 2003Extraarticular manifestations of the joint hypermobility syndrome may include the peripheral nervous system. The purpose of this study was to investigate autonomic function in patients with this syndrome.Forty-eight patients with the joint hypermobility syndrome who fulfilled the 1998 Brighton criteria and 30 healthy control subjects answered a ...
Yael, Gazit +3 more
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Ehlers-Danlos Syndromes, Joint Hypermobility and Hypermobility Spectrum Disorders
2021Ehlers-Danlos syndrome is an umbrella term for a clinically and genetically heterogeneous group of hereditary soft connective tissue disorders mainly featuring abnormal cutaneous texture (doughy/velvety, soft, thin, and/or variably hyperextensible skin), easy bruising, and joint hypermobility.
Lucia, Micale +2 more
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