Literature DB >> 19821143

Clinical and biochemical studies in mucopolysaccharidosis type II carriers.

I V D Schwartz1,2, L L C Pinto3,4, G Breda3, L Lima3, M G Ribeiro5, J G Mota6, A X Acosta7, P Correia8, D D G Horovitz9, C G G Porciuncula10, E Lipinski-Figueiredo10, A C Fett-Conte11, R P Oliveira Sobrinho12, D Y J Norato12, A C Paula13, C A Kim13, A R Duarte14, R Boy15, S Leistner-Segal3, M G Burin3, R Giugliani16,3,4.   

Abstract

The aim of the study was to characterize clinically and biochemically mucopolysaccharidosis type II (MPS II) heterozygotes. Fifty-two women at risk to be a carrier, with a mean age of 34.1 years (range 16-57 years), were evaluated through pedigree analysis, medical history, physical examination, measurement of iduronate sulfatase (IDS) activities in plasma and in leukocytes, quantification of glycosaminoglycans (GAGs) in urine, and analysis of the IDS gene. Eligibility criteria for the study also included being 16 years of age or older and being enrolled in a genetic counselling programme. The pedigree and DNA analyses allowed the identification of 40/52 carriers and 12/52 non-carriers. All women evaluated were clinically healthy, and their levels of urinary GAGs were within normal limits. Median plasma and leukocyte IDS activities found among carriers were significantly lower than the values found for non-carriers; there was, however, an overlap between carriers' and non-carriers' values. Our data suggests that MPS II carriers show lower plasma and leukocyte IDS activities but that this reduction is generally associated neither with changes in levels of urinary GAGs nor with the occurrence of clinical manifestations.

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Year:  2009        PMID: 19821143     DOI: 10.1007/s10545-009-1275-9

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  47 in total

1.  Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 60 obligate carrier females.

Authors:  K D MacDermot; A Holmes; A H Miners
Journal:  J Med Genet       Date:  2001-11       Impact factor: 6.318

2.  Disease manifestations and X inactivation in heterozygous females with Fabry disease.

Authors:  Esther M Maier; Stephanie Osterrieder; Catharina Whybra; Markus Ries; Andreas Gal; Michael Beck; Adelbert A Roscher; Ania C Muntau
Journal:  Acta Paediatr Suppl       Date:  2006-04

3.  Segregation and sporadic cases in families with Hunter's syndrome.

Authors:  G Machill; G Barbujani; G A Danieli; F H Herrmann
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

4.  Urinary glycosaminoglycan excretion in healthy subjects and in patients with mucopolysaccharidoses.

Authors:  M P Gallegos-Arreola; M V Machorro-Lazo; S E Flores-Martínez; G M Zúñiga-González; L E Figuera; A González-Noriega; J Sánchez-Corona
Journal:  Arch Med Res       Date:  2000 Sep-Oct       Impact factor: 2.235

5.  A fluorimetric enzyme assay for the diagnosis of MPS II (Hunter disease).

Authors:  Y V Voznyi; J L Keulemans; O P van Diggelen
Journal:  J Inherit Metab Dis       Date:  2001-11       Impact factor: 4.982

6.  Carrier detection in Hunter syndrome.

Authors:  I M Archer; I D Young; D W Rees; A Oladimeji; F S Wusteman; P S Harper
Journal:  Am J Med Genet       Date:  1983-09

Review 7.  Incidence of the mucopolysaccharidoses in Western Australia.

Authors:  John Nelson; June Crowhurst; Bill Carey; Lawrence Greed
Journal:  Am J Med Genet A       Date:  2003-12-15       Impact factor: 2.802

Review 8.  Female twin with Hunter disease due to nonrandom inactivation of the X-chromosome: a consequence of twinning.

Authors:  B Winchester; E Young; S Geddes; S Genet; J Hurst; H Middleton-Price; N Williams; M Webb; A Habel; S Malcolm
Journal:  Am J Med Genet       Date:  1992-12-01

9.  Fabry disease defined: baseline clinical manifestations of 366 patients in the Fabry Outcome Survey.

Authors:  A Mehta; R Ricci; U Widmer; F Dehout; A Garcia de Lorenzo; C Kampmann; A Linhart; G Sunder-Plassmann; M Ries; M Beck
Journal:  Eur J Clin Invest       Date:  2004-03       Impact factor: 4.686

10.  Diagnosis of Hunter's syndrome carriers; radioactive sulphate incorporation into fibroblasts in the presence or fructose 1-phosphate.

Authors:  T Tønnesen; C Lykkelund; F Güttler
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

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  5 in total

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Authors:  Louise L C Pinto; Taiane A Vieira; Roberto Giugliani; Ida V D Schwartz
Journal:  Orphanet J Rare Dis       Date:  2010-05-28       Impact factor: 4.123

Review 2.  Dosage Compensation in Females with X-Linked Metabolic Disorders.

Authors:  Patrycja Juchniewicz; Ewa Piotrowska; Anna Kloska; Magdalena Podlacha; Jagoda Mantej; Grzegorz Węgrzyn; Stefan Tukaj; Joanna Jakóbkiewicz-Banecka
Journal:  Int J Mol Sci       Date:  2021-04-26       Impact factor: 5.923

3.  Diagnosing Hunter syndrome in pediatric practice: practical considerations and common pitfalls.

Authors:  Barbara K Burton; Roberto Giugliani
Journal:  Eur J Pediatr       Date:  2012-03-01       Impact factor: 3.183

4.  Clinical manifestations in female carriers of mucopolysaccharidosis type II: a Spanish cross-sectional study.

Authors:  Encarna Guillén-Navarro; María Rosario Domingo-Jiménez; Carlos Alcalde-Martín; Ramón Cancho-Candela; María Luz Couce; Enrique Galán-Gómez; Olga Alonso-Luengo
Journal:  Orphanet J Rare Dis       Date:  2013-06-25       Impact factor: 4.123

5.  Mucopolysacccharidoses: From understanding to treatment, a century of discoveries.

Authors:  Roberto Giugliani
Journal:  Genet Mol Biol       Date:  2012-12-18       Impact factor: 1.771

  5 in total

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