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Oral manifestations of 17 patients affected with mucopolysaccharidosis type VI

KANTAPUTRA, Piranit Nik
KANTAPUTRA, Warissara
Tanpaiboon, Pranoot
Uttarilli, Anusha
DALAL, Ashwin
Kayserili, Hulya
Guven, Yeliz
Balci, Mehmet Cihan

Publication date

January 2014

DOI

10.1007/s10545-013-9645-8

Publisher

Springer Science and Business Media LLC

Journal

Journal of Inherited Metabolic Disease

Abstract

To assess oral manifestations of 17 patients with mucopolysaccharidosis type VI (MPS VI) or Maroteaux-Lamy syndrome

Extracted data

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Kisa, Pelin Teke
Kose, Engin

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송주현
장철호
김영재
한세현
이상훈

January 2007

Mucopolysaccharidosis (MPS) is a disorder of storage in which there is excessive accumulation of gly...

The oral manifestations of Maroteaux-Lamy syndrome (mucopolysaccharidosis VI): A case report

Alpoz, AR
Coker, M
Celen, E
Ersin, NK
Gokcen, D
van Diggelenc, OP
Huijmansc, JGM

January 2006

WOS: 000237068400013PubMed ID: 16632276Maroteaux-Lamy syndrome is one of the genetic disorders invol...

Mucopolysaccharidosis: MPS VI and associated delayed tooth eruption

Smith, Kevin S.
Hallett, Kerrod B.
Hall, Roger K.
Wardrop, Robert W.
Firth, Norman

January 1995

Eight cases of mucopolysaccharidosis Type VI (Maroteaux-Lamy syndrome) are reviewed and two cases ar...

Clinical Experiments in Patients with Mucopolysaccharidosis Type VI (Maroteaux-Lamy Syndrome)

Er, Esra
Canda, Ebru
Ucar, Sema Kalkan
Sozmen, Eser
Coker, Mahmut

January 2016

WOS: 000406928300004Aim: Mucopolysaccharidosis (MPS) type VI or Maroteaux Lamy syndrome is an autoso...

Clinical study of 10 Brazilian cases of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome).

Kim, C. A.
Paula, A. C.
Bertola, Debora
Toma, Leny
Giugliani, R.
Moreira, M. B.
Ferraro, V. H.
Albano, Lilian Maria Jose

November 2003

Inst Crianca, Dept Pediat, Sao Paulo, BrazilUNIFESP, Sao Paulo, BrazilUFRGS, Porto Alegre, RS, Brazi...

Management guidelines for mucopolysaccharidosis VI

Giugliani, Roberto

Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome) is a lysosomal storage disease that is characteri...

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Dalal, Ashwin
Balci, Mehmet Cihan
Uttarilli, Anusha
Kayserili, Hulya
Guven, Yeliz
Kantaputra, Piranit Nik
Kantaputra, Warissara
Tanpaiboon, Pranoot
Tananuvat, Napaporn

January 2014

Mucopolysaccharidosis (MPS) type VI or Maroteaux-Lamy syndrome is a very rare autosomal recessive ly...

Dentomaxillofacial manifestations of mucopolysaccharidosis VI: clinical and imaging findings from two cases, with an emphasis on the temporomandibular joint

Cavaleiro, RMD
Pinheiro, MDR
Pinheiro, LR
Tuji, FM
Feio, PDQ
de Souza, ICN
Feio, RHF
de Almeida, SC
Schwartz, IVD
Giugliani, R
Pinheiro, JJV
Santana-Da-Silva, LC

November 2015

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Ci...

Mucopolysaccharidosis VI (Case Report) Brain MRI and MR Spectroscopy Findings

Fuldem Donmez

October 2013

Mucopolysaccharidosis VI or Maroteaux-Lamy syndrome is an autosomal recessive lysosomal storage diso...

Mutational analysis of 105 mucopolysaccharidosis type VI patients

Karageorgos, L.
Brooks, D.
Pollard, A.
Melville, E.
Hein, L.
Clements, P.
Ketteridge, D.
Swiedler, S.
Beck, M.
Giugliani, R.
Harmatz, P.
Wraith, J.
Guffon, N.
Teles, E.
Miranda, C.
Hopwood, J.

January 2007

Mucopolysaccharidosis type VI (MPS VI; Maroteaux-Lamy syndrome) is a lysosomal storage disorder caus...

Clinical Presentation and Follow Up of Patients with Mucopolysaccharidosis Type IVA (Morquio A Disease): Single Center Experience

Ebru Canda
Havva Yazıcı
Esra Er
Cenk Eraslan
Sema Kalkan Uçar
Mahmut Çoker

March 2018

Aim:Mucopolysaccharidosis Type IVA (MPS IVA), Morquio A, is caused by the deficiency in lysosomal en...

Clinical course of sly syndrome (mucopolysaccharidosis type VII).

Montaño, Adriana M
Lock-Hock, Ngu
Steiner, Robert D
Graham, Brett H
Szlago, Marina
Greenstein, Robert
Pineda, Mercedes
Gonzalez-Meneses, Antonio
Çoker, Mahmut
Bartholomew, Dennis
Sands, Mark S
Wang, Raymond
Giugliani, Roberto
Macaya, Alfons
Pastores, Gregory
Ketko, Anastasia K
Ezgü, Fatih
Tanaka, Akemi
Arash, Laila
Beck, Michael
Falk, Rena E
Bhattacharya, Kaustuv
Franco, José
White, Klane K
Mitchell, Grant A
Cimbalistiene, Loreta
Holtz, Max
Sly, William S

February 2016

Mucopolysaccharidosis VII (MPS VII) is an ultra-rare disease characterised by the deficiency of β-gl...

An index case for the attenuated end of the mucopolysaccharidosis type VI clinical spectrum

Brooks, D.
Gibson, G.
Karageorgos, L.
Hein, L.
Robertson, E.
Hopwood, J.

January 2005

Mucopolysaccharidosis type VI (MPS VI, Maroteaux-Lamy syndrome, McKusick #253200) is a lysosomal sto...

Evaluation of Demographic and Clinical Characteristics of Patients with Mucopolysaccharidosis

Atesoglu, Merve
ARSLAN, NUR
Kisa, Pelin Teke
Kose, Engin

June 2017

Aim: Mucopolysaccharidoses (MPSs) are a group of lysosomal storage disorders caused by the deficienc...

Dental findings in Morquio syndrome (Mucopolysaccharidoses Type IVa)

Barker, D
Welbury, Richard

November 2000

Morquio syndrome is a disorder of mucopolysaccharide metabolism with specific skeletal features. The...

뮤코다당증(Mucopolysaccharidosis)환아의 치은 증식

송주현
장철호
김영재
한세현
이상훈

January 2007

Mucopolysaccharidosis (MPS) is a disorder of storage in which there is excessive accumulation of gly...