Literature DB >> 8755171

Bony changes in common mucopolysaccharidoses.

S J Chen1, Y W Li, T R Wang, J C Hsu.   

Abstract

To evaluate the radiological features of mucopolysaccharidoses (MPS), 15 cases were collected for review in this hospital, retrospectively (1985-1995). Eight cases of Hurler syndrome, two cases of Hunter syndrome, two cases of Sanfilippo syndrome and three cases of Morquio syndrome were classified. Varying severity of dysostosis multiplex is the general bony manifestation of MPS, but special appearance may occur in particular types. Hurler syndrome is the prototype of MPS. The main findings were as follows: "J" shaped sella turcica, paddle-like ribs, anterior inferior beaking (hook-like) of lower thoracic-upper lumbar hypoplastic vertebral bodies, flared iliac wings, constrictive iliac bodies, diaphyseal expansion of long bones, distal ulna and radius tilt toward each other, bullet-like proximal phalanges and central pointing of proximal metacarpals. Hunter and Sanfilippo syndromes had the appearance of moderate to mild dysostosis multiplex. Morquio syndrome had distinctive bony changes as vertebral plana and tongue-like protrusion in the anterior part of the lower thoracic-upper lumbar vertebral bodies, particularly short of the distal deformed ulna and poor ossification of the proximal lateral tibial epiphyses. Although clinical presentations and the hallmarks of bony changes helped possible classification of MPS, definite diagnosis depends on enzyme analysis.

Entities:  

Mesh:

Year:  1996        PMID: 8755171

Source DB:  PubMed          Journal:  Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi        ISSN: 0001-6578


  8 in total

1.  Quantifying medical manifestations in Hurler syndrome with the infant physical symptom score: associations with long-term physical and adaptive outcomes.

Authors:  Alia Ahmed; Kyle Rudser; Kelly E King; Julie B Eisengart; Paul J Orchard; Elsa Shapiro; Chester B Whitley
Journal:  Mol Genet Metab       Date:  2022-03-10       Impact factor: 4.204

Review 2.  Mucopolysaccharidoses.

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

3.  Anterior Hypopituitarism and Treatment Response in Hunter Syndrome: A Comparison of Two Patients.

Authors:  Munier A Nour; Paola Luca; David Stephure; Xing-Chang Wei; Aneal Khan
Journal:  Case Rep Pediatr       Date:  2016-11-28

4.  Sella turcica measurements on lateral cephalograms of patients with neurofibromatosis type 1.

Authors:  Reinhard E Friedrich; Johanna Baumann; Anna Suling; Hannah T Scheuer; Hanna A Scheuer
Journal:  GMS Interdiscip Plast Reconstr Surg DGPW       Date:  2017-03-23

Review 5.  Treatment of hip dysplasia in patients with mucopolysaccharidosis type I after hematopoietic stem cell transplantation: results of an international consensus procedure.

Authors:  Eveline J Langereis; Andrea Borgo; Ellen Crushell; Paul R Harmatz; Peter M van Hasselt; Simon A Jones; Paula M Kelly; Christina Lampe; Johanna H van der Lee; Thierry Odent; Ralph Sakkers; Maurizio Scarpa; Matthias U Schafroth; Peter A Struijs; Vassili Valayannopoulos; Klane K White; Frits A Wijburg
Journal:  Orphanet J Rare Dis       Date:  2013-10-03       Impact factor: 4.123

Review 6.  Pain in Mucopolysaccharidoses: Analysis of the Problem and Possible Treatments.

Authors:  Sabrina Congedi; Marcello Orzalesi; Chiara Di Pede; Franca Benini
Journal:  Int J Mol Sci       Date:  2018-10-08       Impact factor: 5.923

7.  Diagnosis of Mucopolysaccharidosis Based on History and Clinical Features: Evidence from the Bajio Region of Mexico.

Authors:  Douglas Colmenares-Bonilla; Christian Colin-Gonzalez; Alejandra Gonzalez-Segoviano; Enrique Esquivel Garcia; Ma Martha Vela-Huerta; Fanny Guadalupe Lopez-Gomez
Journal:  Cureus       Date:  2018-11-20

Review 8.  Mucopolysaccharidosis Type I.

Authors:  Francyne Kubaski; Fabiano de Oliveira Poswar; Kristiane Michelin-Tirelli; Ursula da Silveira Matte; Dafne D Horovitz; Anneliese Lopes Barth; Guilherme Baldo; Filippo Vairo; Roberto Giugliani
Journal:  Diagnostics (Basel)       Date:  2020-03-16
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.