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Ehlers-Danlos syndromes: Revised nosology, Villefranche, 1997
Overview
Integrity signals
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Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“This genetic disorder is present in at least 1/5000 individuals [1] and an important cause of joint hypermobility syndrome [2].”
In the citing paper
“Further, the Swedish Patient Registry does not distinguish between various forms of EDS, and we were unable to examine psychiatric disorders and EDS divided into classical (type I) or vascular (type IV) or according to the newer Villefranche Classification of EDS [2].”
In the citing paper
“This classification delineated six subtypes, for which major and minor clinical criteria were defined, and which included the biochemical and molecular basis, when known.”
From The 2017 international classification of the Ehlers–Danlos syndromes (2017) · cites this paper as Beighton et al., 1998
In the citing paper
“Over the past two decades, the Villefranche Nosology, which delineated six subtypes, has been widely used as the standard for clinical diagnosis of EDS.”
From The 2017 international classification of the Ehlers–Danlos syndromes (2017) · cites this paper as Beighton et al., 1998
In the citing paper
“With the elucidation of the biochemical and molecular basis of many of these EDS types, a revised classification, the ' Villefranche Nosology, ' was published in 1998 [Beighton et al., 1998].”
From The 2017 international classification of the Ehlers–Danlos syndromes (2017) · cites this paper as Beighton et al., 1998
In the citing paper
“The Villefranche EDS nosology group noted these difficulties in distinguishing this rare disorder from other hereditary disorders of connective tissue [Beighton et al., 1998].”
From The Ehlers–Danlos syndromes, rare types (2017) · cites this paper as Beighton et al., 1998
In the citing paper
“which is much higher than the previously estimated 1 in 5000 rate of all hypermobile EDS types combined. 14”
From High-Throughput Screening for CYP21A1P-TNXA/TNXB Chimeric Genes Responsible for Ehlers Danlos Syndrome in Patients with Congenital Adrenal Hyperplasia. (2019) · cites this paper as [14]
In the citing paper
“The diagnosis of EDS due to CAH-X relies mainly on clinical evaluations, such as physical examination for joint hypermobility, skin characteristics, and imaging. 14”
From High-Throughput Screening for CYP21A1P-TNXA/TNXB Chimeric Genes Responsible for Ehlers Danlos Syndrome in Patients with Congenital Adrenal Hyperplasia. (2019) · cites this paper as [14]
In the citing paper
“EDS is the most common non‐inflammatory connective tissue disorder featuring joint hypermobility, with the hypermobile EDS (hEDS) subtype representing 80–90% of the burden of disease.”
From Hypermobile Ehlers–Danlos syndrome and disorders of the gastrointestinal tract: What the gastroenterologist needs to know (2022) · cites this paper as [1]
In the citing paper
“EDS is the most common non‐inflammatory connective tissue disorder featuring joint hypermobility, with the hypermobile EDS (hEDS) subtype representing 80–90% of the burden of disease.”
From Hypermobile Ehlers–Danlos syndrome and disorders of the gastrointestinal tract: What the gastroenterologist needs to know (2022) · cites this paper as [1]
In the citing paper
“The diagnosis of JHS and EDS-HT was established by applying published diagnostic criteria.”
In the citing paper
“This new set of clinical criteria is stricter than the previous Villefranche criteria, used for the diagnosis of EDS hypermobility type (EDS-HT) [2], and the Brighton criteria for joint hypermobility syndrome (JHS) [3].”
Citations
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Research works printed but not linked: 23
- Arneson, 1980, JAMA, 244, 144, 10.1001/jama.1980.03310020020019 · DOI
- (1970): ?The Ehlers-Danlos Syndrome.? London: William Heinemann Medical Books, pp 1-194.
- (1993): The Ehlers-Danlos syndromes. In (ed) ?Heritable Disorders of Connective Tissue,? 5th ed. St. Louis: Mosby, pp 189-251.
- Beighton, 1985, Clin Genet, 27, 472, 10.1111/j.1399-0004.1985.tb00234.x · DOI
- Beighton, 1960, Br J Surg, 56, 255, 10.1002/bjs.1800560404 · DOI
- Beighton, 1969, J Bone Joint Surg [Br], 51, 444, 10.1302/0301-620X.51B3.444 · DOI
- (1989): ?Hypermobility of Joints,? 2nd edition. Berlin: Springer, pp 1-182. · DOI · Paper page
- Devereux, 1987, Am Heart J, 113, 1265, 10.1016/0002-8703(87)90955-0 · DOI
- Hausser, 1994, Hum Genet, 93, 394, 10.1007/BF00201664 · DOI
- Leier, 1980, Ann Intern Med, 92, 171, 10.7326/0003-4819-92-2-171 · DOI
- (1972): The Ehlers-Danlos syndrome. In: ?Heritable Disorders of Connective Tissue,? 4th ed. St. Louis: C.V. Mosby, pp 292-371.
- Pepin, 1992, Am J Hum Genet, 51, 44
- Roman, 1989, Am J Cardiol, 64, 507, 10.1016/0002-9149(89)90430-X · DOI
- Roman, 1993, J Am Coll Cardiol, 22, 1470, 10.1016/0735-1097(93)90559-J · DOI
- Sacheti, 1997, J Pain Symptom Managem, 14, 88, 10.1016/S0885-3924(97)00007-9 · DOI
- Sorokin, 1994, J Reprod Med, 39, 281
- Steinmann, 1989, Am J Med Genet, 34, 68, 10.1002/ajmg.1320340113 · DOI
- (1993): The Ehlers-Danlos syndrome. In (ed): ?Connective Tissue and its Heritable Disorders: Molecular, Genetic and Medical Aspects.? New York: Wiley-Liss, pp 351-407.
- Steinmann, 1995, Am J Hum Genet, 57, 1505
- (1977): A New Variant of Ehlers-Danlos Syndrome: An Autosomal Dominant Disorder of Fragile Skin, Abnormal Scarring and Generalized Periodontitis. BD: OAS XIII (3B):85-93.
- Vogel, 1979, Lab Invest, 40, 201
- Wenstrup, 1989, J Pediatr, 115, 405, 10.1016/S0022-3476(89)80839-X · DOI · Paper page
- Wolf, 1990, Arthritis Rheum, 33, 160, 10.1002/art.1780330203 · DOI · Paper page
Metadata
- Authors
- Beighton, P., Paepe, A. D., Steinmann, B., Tsipouras, P., & Wenstrup, R. J.
- Venue
- American Journal of Medical Genetics
- Publisher
- Wiley
- Published
- 1998-04-28
- Volume
- 77
- Issue
- 1
- Pages
- 31-37
- ISSN
- 0148-7299
- 1096-8628
- Language
- en
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- CoChat. (2026). Citation check: Ehlers-Danlos syndromes: Revised nosology, Villefranche, 1997. https://app.cochat.ai/papers/10.1002/(sici)1096-8628(19980428)77:1
- The paper
- Beighton, P., Paepe, A. D., Steinmann, B., Tsipouras, P., & Wenstrup, R. J. (1998). Ehlers-Danlos syndromes: Revised nosology, Villefranche, 1997. American Journal of Medical Genetics. https://doi.org/10.1002/(sici)1096-8628(19980428)77%3A1
