Volume 56, Issue 4 pp. 520-525
Original Article

Mucopolysaccharidosis type VI in Russia, Kazakhstan, and Central and Eastern Europe

Agnieszka Jurecka

Corresponding Author

Agnieszka Jurecka

Department of Medical Genetics, Children's Memorial Health Institute, Warsaw, Poland

Department of Genetics, University of Gdańsk, Gdańsk, Poland

Correspondence: Agnieszka Jurecka, MD PhD, Department of Genetics, University of Gdańsk, ul. Wita Stwosza 59, 80-308 Gdańsk, Poland. Email: [email protected]Search for more papers by this author
Ekaterina Zakharova

Ekaterina Zakharova

Department of Inherited Metabolic Diseases, Research Center for Medical Genetics, Moscow, Russian Federation

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Loreta Cimbalistiene

Loreta Cimbalistiene

Center for Medical Genetics, Santariskiu Klinikos, Vilnius University Hospital, Vilnius, Lithuania

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Nina Gusina

Nina Gusina

Genetics Unit, National Medical Center “Mother and Child”, Minsk, Belarus

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Vera Malinova

Vera Malinova

Department of Pediatrics and Adolescence Medicine, First Faculty of Medicine, General University Hospital, Charles University, Prague, Czech Republic

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Agnieszka Różdżyńska-Świątkowska

Agnieszka Różdżyńska-Świątkowska

Anthropology Laboratory, Children's Memorial Health Institute, Warsaw, Poland

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Adam Golda

Adam Golda

Department of Cardiology, Gliwice General Hospital, Gliwice, Poland

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Anna Kulpanovich

Anna Kulpanovich

Genetics Unit, National Medical Center “Mother and Child”, Minsk, Belarus

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Gulnara Kaldenovna Abdilova

Gulnara Kaldenovna Abdilova

Department of Pediatrics, Research Center of Pediatrics and Pediatric Surgery, Almaty, Kazakhstan

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Elena Voskoboeva

Elena Voskoboeva

Department of Inherited Metabolic Diseases, Research Center for Medical Genetics, Moscow, Russian Federation

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Anna Tylki-Szymańska

Anna Tylki-Szymańska

Department of Pediatrics, Nutrition and Metabolic Diseases, Children's Memorial Health Institute, Warsaw, Poland

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First published: 26 December 2013
Citations: 20

Abstract

Background

The aim of this study was to describe the natural clinical course, incidence and prevalence of mucopolysaccharidosis type VI (MPS VI) in Russia, Kazakhstan, and Central and Eastern Europe.

Methods

Patients (n = 49) were identified by retrieving the data from eight international centers for MPS VI.

Results

A large number of patients presented with an attenuated phenotype (33%). Height and genotype were related to the severity of the disease, while no clear trend was observed between height and urinary glycosaminoglycan level. A high prevalence of the p.R152W mutation was observed both in the whole series (42%) as well as in Russian patients (43%). The incidence rate ranged from 0.0363 to 0.64 per 100 000 live births in Poland and Lithuania, respectively.

Conclusions

The observed high p.R152W carrier frequency in the Lithuanian population may indicate a possible founder effect in this region. The high prevalence of this mutation observed in the whole series, as well as the Slavic origin of the majority of patients homozygous for this mutation, suggest that p.R152W may be of Slavic, not Lithuanian origin. Resettlement of the Polish population after World War II resulted in dilution of the prevalence of carriers in Poland and a very low MPS VI incidence.

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