Literature DB >> 3114705

Radiological findings in patients with mucopolysaccharidosis I H/S (Hurler-Scheie syndrome).

H Schmidt, K Ullrich, H J von Lengerke, M Kleine, J Brämswig.   

Abstract

The development of radiological changes in two patients with mucopolysaccharidosis (MPS) Type I H/S is described. Radiological findings reveal enlargement of the sella in one patient, impression of the basilar skull in the other patient. Sclerosis and thickening of the base of skull was observed in both patients. The mandibular necks were short with striking flattening of the superior surfaces of the condyles, when the patients reached adult age. At the age of 12, hypertelorism and spaced teeth were already present in both patients. In addition, they showed early costal, clavicular and scapular changes, irregularities of the acromial joints and acetabulae, hypoplasia of the inferior portion of the iliac bones and flared iliac wings. The flat femurs had short metaphyses and were held in valgus position. Development of dentigerous cysts as well as mandibular changes seem to be rather specific for this variant of alpha-L-iduronidase deficiency. In contrast to the classical form of MPS I, skeletal changes of the spine and hands are minimal.

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Year:  1987        PMID: 3114705     DOI: 10.1007/bf02396619

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN: 0301-0449


  14 in total

1.  Hurler/Scheie genetic compound (mucopolysaccharidosis IH/IS) in Japanese brothers.

Authors:  T Kajii; I Matsuda; T Osawa; H Katsunuma; T Ichida
Journal:  Clin Genet       Date:  1974       Impact factor: 4.438

2.  Letter: Chondroitinsulphaturia with alpha-L-iduronidase deficiency.

Authors:  J Spranger; J Gehler; J F O'Brien; M Cantz
Journal:  Lancet       Date:  1974-11-02       Impact factor: 79.321

3.  Allelism, non-allelism, and genetic compounds among the mucopolysaccharidoses.

Authors:  V A McKusick; R R Howell; I E Hussels; E F Neufeld; R E Stevenson
Journal:  Lancet       Date:  1972-05-06       Impact factor: 79.321

4.  Spastic quadriparesis due to C1-C2 subluxation in Hurler syndrome.

Authors:  C B Brill; J S Rose; L Godmilow; S Sklower; J Willner; K Hirschhorn
Journal:  J Pediatr       Date:  1978-03       Impact factor: 4.406

5.  Variant of iduronidase deficient mucopolysaccharidoses: further evidence for genetic heterogeneity.

Authors:  B S Danes
Journal:  J Med Genet       Date:  1977-10       Impact factor: 6.318

6.  Chondroitin-4-sulfate mucopolysaccharidosis.

Authors:  J W Spranger; W Schuster; F Freitag
Journal:  Helv Paediatr Acta       Date:  1971-10

7.  Mucopolysaccharidosis (type I Hurler-Scheie compound).

Authors:  A E Lorinez; L F Montes
Journal:  J Cutan Pathol       Date:  1975       Impact factor: 1.587

8.  [Chondroitin-4-sulfate mucopolysaccharidosis].

Authors:  W Schuster; J Spranger
Journal:  Monatsschr Kinderheilkd       Date:  1971-07

9.  alpha-L-iduronidase deficiency and possible Hurler-Scheie genetic compound. Clinical, pathologic, and biochemical findings.

Authors:  P R Winters; M J Harrod; S A Molenich-Heetred; J Kirkpatrick; R N Rosenberg
Journal:  Neurology       Date:  1976-11       Impact factor: 9.910

10.  The iduronidase-deficient mucopolysaccharidoses: clinical and roentgenorgraphic features.

Authors:  R E Stevenson; R R Howell; V A McKusick; R Suskind; J W Hanson; D E Elliott; E F Neufeld
Journal:  Pediatrics       Date:  1976-01       Impact factor: 7.124

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  12 in total

1.  [Mucopolysaccharidoses].

Authors:  B Link; E Miebach; T Vetter; D Schmitt; M Beck; A Meurer
Journal:  Orthopade       Date:  2008-01       Impact factor: 1.087

2.  The oral health needs of children, adolescents and young adults affected by a mucopolysaccharide disorder.

Authors:  Alison James; Christian J Hendriksz; Owen Addison
Journal:  JIMD Rep       Date:  2011-09-06

3.  Differences in maxillomandibular morphology among patients with mucopolysaccharidoses I, II, III, IV and VI: a retrospective MRI study.

Authors:  Till Koehne; Anja Köhn; Reinhard E Friedrich; Uwe Kordes; Thorsten Schinke; Nicole Muschol; Bärbel Kahl-Nieke
Journal:  Clin Oral Investig       Date:  2017-10-18       Impact factor: 3.573

4.  Legg-Perthes disease-like joint involvement and diagnosis delay in Scheie syndrome: a case report.

Authors:  Meltem Alkan Melikoglu; Hilal Kocabas; Ilhan Sezer; Hasan Fatih Cay; Aysegul Guller Cassidy; Nilufer Balci
Journal:  Clin Rheumatol       Date:  2007-01-31       Impact factor: 2.980

5.  Mucopolysaccharidosis: thickening of dura mater at the craniocervical junction and other CT/MRI findings.

Authors:  A Taccone; P Tortori Donati; A Marzoli; A Dell'Acqua; R Gatti; D Leone
Journal:  Pediatr Radiol       Date:  1993

Review 6.  Mucopolysaccharidoses.

Authors:  Rolando Cimaz; Francesco La Torre
Journal:  Curr Rheumatol Rep       Date:  2014-01       Impact factor: 4.592

7.  Low bone mineral content and challenges in interpretation of dual-energy X-ray absorptiometry in children with mucopolysaccharidosis types I, II, and VI.

Authors:  Lynda E Polgreen; William Thomas; Ellen Fung; David Viskochil; David A Stevenson; Julia Steinberger; Paul Orchard; Chester B Whitley; Kristine E Ensrud
Journal:  J Clin Densitom       Date:  2013-04-02       Impact factor: 2.617

8.  Oral manifestations of 17 patients affected with mucopolysaccharidosis type VI.

Authors:  Piranit Nik Kantaputra; Hülya Kayserili; Yeliz Güven; Warissara Kantaputra; Mehmet C Balci; Pranoot Tanpaiboon; Anusha Uttarilli; Ashwin Dalal
Journal:  J Inherit Metab Dis       Date:  2013-08-22       Impact factor: 4.982

9.  Mucopolysaccharidosis type I Hurler-Scheie syndrome: A rare case report.

Authors:  Ramesh Tatapudi; M Gunashekhar; P Suryanarayana Raju
Journal:  Contemp Clin Dent       Date:  2011-01

10.  alpha-L-iduronidase therapy for mucopolysaccharidosis type I.

Authors:  Jakub Tolar; Paul J Orchard
Journal:  Biologics       Date:  2008-12
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