Literature DB >> 2260589

Phenotypic overlap of Ehlers-Danlos syndrome types IV and VIII.

J K Hartsfield1, B G Kousseff.   

Abstract

An 18-year-old Caucasian woman has been followed since age 12 years for Ehlers-Danlos syndrome (EDS) with easy bruisability and "cigarette paper scars." Her chief complaint at age 17 years was tooth mobility, especially in the anterior mandible, necessitating the removal of the four incisors. Initial biochemical analysis of cultured skin fibroblasts indicated the presence of pepsin-sensitive type III collagen. Subsequent analysis of cultured skin fibroblasts by the same laboratory and another laboratory found no abnormality in the type III collagen with or without protease treatment. This is in distinction to the finding of abnormal type III collagen in the only two reported patients with EDS and early-onset periodontitis who have had collagen analyses. One of them was diagnosed as EDS type IV and the other as EDS type VIII, although the defects of type III collagen were consistent with EDS type IV. The defect in type III collagen in some patients with early periodontitis and the considerable overlap of the clinical manifestations of EDS types IV and VIII point out the need for further studies of collagen formation and maturation in any patient who has early periodontitis and who has been classified with EDS type IV or VIII.

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Year:  1990        PMID: 2260589     DOI: 10.1002/ajmg.1320370408

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  10 in total

1.  Ehlers-Danlos syndrome with severe early-onset periodontal disease (EDS-VIII) is a distinct, heterogeneous disorder with one predisposition gene at chromosome 12p13.

Authors:  Nazneen Rahman; Melanie Dunstan; M Dawn Teare; Sandra Hanks; Jenny Douglas; Kim Coleman; William E Bottomly; Mary E Campbell; Britta Berglund; Magnus Nordenskjöld; Bengt Forssell; Nigel Burrows; Peter Lunt; Ian Young; Nigel Williams; Graham R Bignell; P Andrew Futreal; F Michael Pope
Journal:  Am J Hum Genet       Date:  2003-05-29       Impact factor: 11.025

Review 2.  Ehlers-Danlos syndrome (EDS) type IV: review of the literature.

Authors:  Cristiano Macabu Badauy; Sabrina S Gomes; Manoel Sant'Ana Filho; José Artur Bogo Chies
Journal:  Clin Oral Investig       Date:  2007-01-13       Impact factor: 3.573

Review 3.  Ehlers-Danlos syndrome has varied molecular mechanisms.

Authors:  F M Pope; N P Burrows
Journal:  J Med Genet       Date:  1997-05       Impact factor: 6.318

4.  Ehlers-Danlos syndrome type VIII is clinically heterogeneous disorder associated primarily with periodontal disease, and variable connective tissue features.

Authors:  Eyal Reinstein; Celia Dawn DeLozier; Ziv Simon; Serguei Bannykh; David L Rimoin; Cynthia J Curry
Journal:  Eur J Hum Genet       Date:  2012-06-27       Impact factor: 4.246

5.  Ehlers danlos syndrome - a case report.

Authors:  Pragati Kaurani; Nikhil Marwah; Mayank Kaurani; Narendra Padiyar
Journal:  J Clin Diagn Res       Date:  2014-03-15

6.  Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutation.

Authors:  T C Hart; P S Hart; M D Michalec; Y Zhang; M L Marazita; M Cooper; O M Yassin; M Nusier; S Walker
Journal:  J Med Genet       Date:  2000-02       Impact factor: 6.318

7.  Periodontal conditions in Williams Beuren syndrome: a series of 8 cases.

Authors:  C Joseph; M M Landru; F Bdeoui; B Gogly; S M Dridi
Journal:  Eur Arch Paediatr Dent       Date:  2008-09

8.  Ehlers-Danlos Syndrome Type VIII: A Rare Cause of Leg Ulcers in Young Patients.

Authors:  Sophie Ronceray; Juliette Miquel; Antoine Lucas; Gérald E Piérard; Trinh Hermanns-Lê; Anne De Paepe; Alain Dupuy
Journal:  Case Rep Dermatol Med       Date:  2013-10-03

9.  Fatal Ruptured Blood Blister-like Aneurysm of Middle Cerebral Artery Associated with Ehlers-Danlos Syndrome Type VIII (Periodontitis Type).

Authors:  Ulaş Cıkla; Alireza Sadighi; Andrew Bauer; Mustafa K Başkaya
Journal:  J Neurol Surg Rep       Date:  2014-08-11

10.  Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S, which Encode Subcomponents C1r and C1s of Complement.

Authors:  Ines Kapferer-Seebacher; Melanie Pepin; Roland Werner; Timothy J Aitman; Ann Nordgren; Heribert Stoiber; Nicole Thielens; Christine Gaboriaud; Albert Amberger; Anna Schossig; Robert Gruber; Cecilia Giunta; Michael Bamshad; Erik Björck; Christina Chen; David Chitayat; Michael Dorschner; Marcus Schmitt-Egenolf; Christopher J Hale; David Hanna; Hans Christian Hennies; Irene Heiss-Kisielewsky; Anna Lindstrand; Pernilla Lundberg; Anna L Mitchell; Deborah A Nickerson; Eyal Reinstein; Marianne Rohrbach; Nikolaus Romani; Matthias Schmuth; Rachel Silver; Fulya Taylan; Anthony Vandersteen; Jana Vandrovcova; Ruwan Weerakkody; Margaret Yang; F Michael Pope; Peter H Byers; Johannes Zschocke
Journal:  Am J Hum Genet       Date:  2016-10-13       Impact factor: 11.025

  10 in total

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