نتایج جستجو برای: mucopolysaccharidosis type

تعداد نتایج: 1343233  

2014
Mehwish Farrukh Ayesha Haque

Mucopolysaccharidosis (MPS) are a group of metabolic disorders of the lysosomal storage disease family caused by the absence or malfunctioning of lysosomal enzymes, which blocks degradation of mucopolysaccharides and leads to abnormal accumulation of heparan sulfate, dermatan sulfate, and keratan sulfate. Morquio’s syndrome is a rare autosomal-recessive mucopolysaccharidosis. This syndrome is c...

Journal: :The Biochemical journal 1985
J J Hopwood H Elliott

Sulphated N-acetylhexosamines have been isolated from human urine and tentatively identified as N-acetylglucosamine 6-sulphate (GlcNAc6S), N-acetylgalactosamine 6-sulphate (GalNAc6S), N-acetylgalactosamine 4-sulphate (GalNAc4S) and N-acetylgalactosamine 4,6-disulphate (GalNAc4,6diS). Urine from mucopolysaccharidosis-Type-IIID, -IVA and -VI patients compared with that from normal individuals con...

2017
Yasuhiro Chikaishi Kenichi Kobayashi Shuichi Shinohara Akihiro Taira Yusuke Nabe Shinji Shinohara Taiji Kuwata Masaru Takenaka Soichi Oka Ayako Hirai Kazue Yoneda Koji Kuroda Naoko Imanishi Yoshinobu Ichiki Fumihiro Tanaka

Background Treatment of tracheostenosis after tracheostomy in pediatric patients is often difficult. Mucopolysaccharidosis is a lysosomal storage disease that may induce obstruction of the airways. Case Presentation A 16-year-old male patient underwent long-term follow-up after postnatal diagnosis of type II mucopolysaccharidosis. At 11 years of age, tracheostomy was performed for mucopolysac...

Journal: :AJNR. American journal of neuroradiology 1995
M Vinchon A Cotten J Clarisse R Chiki J L Christiaens

We present a case of type II mucopolysaccharidosis in which the diagnosis was delayed until the onset of cervical myelopathy in adulthood. Radiographic features were characteristic, with striking dural thickening shown on CT and MR imaging.

2011
S. O'hEireamhoin T. Bayer K. J. Mulhall

Children affected by mucopolysaccharidosis (MPS) type IH (Hurler Syndrome), an autosomal recessive metabolic disorder, are known to experience a range of musculoskeletal manifestations including spinal abnormalities, hand abnormalities, generalised joint stiffness, genu valgum, and hip dysplasia and avascular necrosis. Enzyme therapy, in the form of bone marrow transplantation, significantly in...

2010
Gauri Shankar Shah Tania Mahal Subodh Sharma

INTRODUCTION We present a very rare case of mucopolysaccharidosis with atypical presentation such as mild mental retardation, an acrocephalic head and no corneal clouding. The purpose of presenting this case is to highlight the distinctive manifestation of mucopolysaccharidosis type II (Hunter syndrome). CASE PRESENTATION A 10-year-old East Asian boy presented with abdominal distension of fiv...

Journal: :Brazilian journal of otorhinolaryngology 2016
Çağıl Gökdoğan Şenay Altinyay Ozan Gökdoğan Hakan Tutar Bülent Gündüz İlyas Okur Leyla Tümer Yusuf Kemal Kemaloğlu

INTRODUCTION Mucopolysaccharidosis is a hereditary lysosomal storage disease, which develops due to a deficiency in the enzymes that play a role in the metabolism of glycosaminoglycans (GAG). The incidence of mucopolysaccharidosis is 1/25,000, with autosomal recessive inheritance (except for MPS II). Mucopolysaccharidosis occurs in seven different types, each with a different congenital deficie...

Journal: :N.N. Priorov Journal of Traumatology and Orthopedics 2018

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