Literature DB >> 23110520

The Kid-Short Marfan Score (Kid-SMS) - an easy executable risk score for suspected paediatric patients with Marfan syndrome.

Goetz C Mueller1, Veronika Stark, Kristoffer Steiner, Jochen Weil, Yskert von Kodolitsch, Thomas S Mir.   

Abstract

AIM: Due to age-dependent manifestations, diagnosis of Marfan syndrome (MFS) in children and adolescents is sophisticated. Although revised Ghent criteria is a major step forward, its utility in children is still restricted due to expensive and technically advanced diagnostics. As early diagnosis submits long-term benefits concerning prognosis, the need of an appropriate diagnostic tool for risk stratification of suspected paediatric patients with Marfan is justified. METHODS AND
RESULTS: Sixty paediatric patients with Marfan were subject to a standardized diagnostic programme. All clinical symptoms of the revised Ghent nosology were analysed concerning age at first clinical manifestation, prevalence and likelihood ratio for MFS. Symptoms with early onset, high prevalence and high positive likelihood ratio were identified and combined for a risk score called Kid-Short Marfan Score (Kid-SMS). Three risk categories for suspicion of Marfan syndrome were developed. Finally, the Kid-SMS was operated in 130 paediatric patients with suspected MFS. Kid-SMS identified significantly more suspected patients with Marfan compared with Ghent nosology, revised Ghent and genetics alone without oversensitivity.
CONCLUSION: Whereas diagnosis of MFS in childhood is sophisticated, Kid-SMS is a useful tool for risk stratification of suspected paediatric patients with Marfan by easy executable diagnostics, especially for paediatricians and paediatric cardiologists. ©2012 The Author(s)/Acta Paediatrica ©2012 Foundation Acta Paediatrica.

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Mesh:

Year:  2012        PMID: 23110520     DOI: 10.1111/apa.12072

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN: 0803-5253            Impact factor:   2.299


  10 in total

1.  The transition of pediatric Marfan patients to adult care: a challenge and its risks.

Authors:  Veronika C Stark; Katrin Doering; Yskert von Kodolitsch; Rainer Kozlik-Feldmann; Götz C Mueller; Jakob Olfe; Meike Rybczynski; Helke Schueler; Thomas S Mir
Journal:  Cardiovasc Diagn Ther       Date:  2018-12

Review 2.  Perspectives on the revised Ghent criteria for the diagnosis of Marfan syndrome.

Authors:  Yskert von Kodolitsch; Julie De Backer; Helke Schüler; Peter Bannas; Cyrus Behzadi; Alexander M Bernhardt; Mathias Hillebrand; Bettina Fuisting; Sara Sheikhzadeh; Meike Rybczynski; Tilo Kölbel; Klaus Püschel; Stefan Blankenberg; Peter N Robinson
Journal:  Appl Clin Genet       Date:  2015-06-16

Review 3.  The role of the multidisciplinary health care team in the management of patients with Marfan syndrome.

Authors:  Yskert von Kodolitsch; Meike Rybczynski; Marina Vogler; Thomas S Mir; Helke Schüler; Kerstin Kutsche; Georg Rosenberger; Christian Detter; Alexander M Bernhardt; Axel Larena-Avellaneda; Tilo Kölbel; E Sebastian Debus; Malte Schroeder; Stephan J Linke; Bettina Fuisting; Barbara Napp; Anna Lena Kammal; Klaus Püschel; Peter Bannas; Boris A Hoffmann; Nele Gessler; Eva Vahle-Hinz; Bärbel Kahl-Nieke; Götz Thomalla; Christina Weiler-Normann; Gunda Ohm; Stefan Neumann; Dieter Benninghoven; Stefan Blankenberg; Reed E Pyeritz
Journal:  J Multidiscip Healthc       Date:  2016-11-03

4.  Orthopaedic Aspects of Marfan Syndrome: The Experience of a Referral Center for Diagnosis of Rare Diseases.

Authors:  Fernando De Maio; Alessandro Fichera; Vincenzo De Luna; Federico Mancini; Roberto Caterini
Journal:  Adv Orthop       Date:  2016-12-05

5.  Exome sequencing identifies de novo pathogenic variants in FBN1 and TRPS1 in a patient with a complex connective tissue phenotype.

Authors:  Diane B Zastrow; Patricia A Zornio; Annika Dries; Jennefer Kohler; Liliana Fernandez; Daryl Waggott; Magdalena Walkiewicz; Christine M Eng; Melanie A Manning; Ellyn Farrelly; Paul G Fisher; Euan A Ashley; Jonathan A Bernstein; Matthew T Wheeler
Journal:  Cold Spring Harb Mol Case Stud       Date:  2017-01

6.  Kid-Short Marfan Score (Kid-SMS) Is a Useful Diagnostic Tool for Stratifying the Pre-Test Probability of Marfan Syndrome in Childhood.

Authors:  Veronika C Stark; Florian Arndt; Gesa Harring; Yskert von Kodolitsch; Rainer Kozlik-Feldmann; Goetz C Mueller; Kristoffer J Steiner; Thomas S Mir
Journal:  Diseases       Date:  2015-03-12

Review 7.  When flexibility is not necessarily a virtue: a review of hypermobility syndromes and chronic or recurrent musculoskeletal pain in children.

Authors:  Marco Cattalini; Raju Khubchandani; Rolando Cimaz
Journal:  Pediatr Rheumatol Online J       Date:  2015-10-06       Impact factor: 3.054

Review 8.  A scoping review presenting a wide variety of research on paediatric and adolescent patients with Marfan syndrome.

Authors:  Ingeborg Beate Lidal; Trine Bathen; Heidi Johansen; Gry Velvin
Journal:  Acta Paediatr       Date:  2020-02-17       Impact factor: 2.299

Review 9.  Diagnosis support systems for rare diseases: a scoping review.

Authors:  Carole Faviez; Xiaoyi Chen; Nicolas Garcelon; Antoine Neuraz; Bertrand Knebelmann; Rémi Salomon; Stanislas Lyonnet; Sophie Saunier; Anita Burgun
Journal:  Orphanet J Rare Dis       Date:  2020-04-16       Impact factor: 4.123

10.  How to Distinguish Marfan Syndrome from Marfanoid Habitus in a Physical Examination-Comparison of External Features in Patients with Marfan Syndrome and Marfanoid Habitus.

Authors:  Lidia Wozniak-Mielczarek; Michalina Osowicka; Alicja Radtke-Lysek; Magda Drezek-Nojowicz; Natasza Gilis-Malinowska; Anna Sabiniewicz; Maksymilian Mielczarek; Robert Sabiniewicz
Journal:  Int J Environ Res Public Health       Date:  2022-01-11       Impact factor: 3.390

  10 in total

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