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921 Possible Causes for Mucopolysaccharidosis 2

  • Mucopolysaccharidosis 2

    Mucopolysaccharidosis 2 presents with a progressive multisystem involvement due to glycosaminoglycan accumulation in virtually all tissues and organs.[symptoma.com] Differential diagnosis Differential diagnoses include mucopolysaccharidosis type 1, 6, 7; sialidosis type 2; mucolipidosis type 2 and 3; and multiple sulfatase deficiency.[orpha.net] 2 Mucopolysaccharidosis MPS-I-H Mucopolysaccharidosis MPS-I-H/S Mucopolysaccharidosis MPS-II Mucopolysaccharidosis MPS-I-S Mucopolysaccharidosis MPS-IV-A Mucopolysaccharidosis[icd9data.com]

  • Mucopolysaccharidosis

    Differential diagnosis Differential diagnoses include mucopolysaccharidosis type 1, 6, 7; sialidosis type 2; mucolipidosis type 2 and 3; and multiple sulfatase deficiency.[orpha.net] 2 Mucopolysaccharidosis MPS-I-H Mucopolysaccharidosis MPS-I-H/S Mucopolysaccharidosis MPS-II Mucopolysaccharidosis MPS-I-S Mucopolysaccharidosis MPS-IV-A Mucopolysaccharidosis[icd9data.com] KEYWORDS: X chromosome inactivation; X;autosome translocation; female Hunter syndrome; iduronate 2-sulfatase; mucopolysaccharidosis type II; skewed[ncbi.nlm.nih.gov]

  • Mucopolysaccharidosis 6

    1 mucopolysaccharidosis Англо-русский офтальмологический словарь mucopolysaccharidosis 2 mucopolysaccharidosis Англо-русский толковый словарь генетических терминов mucopolysaccharidosis[translate.academic.ru] The patient represents relatively attenuated MPS VI with osteo-articular and cardiac changes (Table I, II, Figure 1, 2). keywords: mucopolysaccharidosis type VI, Maroteaux-Lamy[termedia.pl] Oral manifestations of 17 patients affected with mucopolysaccharidosis type VI. J Inherit Metab Dis. 2014 Mar. 37(2):263-8. [Medline].[emedicine.medscape.com]

  • Mucopolysaccharidosis 7

    1H/S (IDUA) * Sequencing (complete) EDTA blood / DNA 2-3 weeks Mucopolysaccharidosis 2 (IDS) * Sequencing (complete) & MLPA EDTA blood 2-3 weeks Mucopolysaccharidosis 3A[diagenom.de] Bone marrow transplantation for mucopolysaccharidosis type I: experience of two British centres. Arch Dis Child. 1997 Feb. 76(2):92-9. [Medline].[emedicine.medscape.com] Enrollment in Phase 3 Study of Recombinant Human Beta-Glucuronidase in Mucopolysaccharidosis Type 7 (link) Ultragenyx Announces Positive 36-Week Data From Phase 1/2 Study[ultragenyx.com]

  • Mucopolysaccharidosis 4A

    1H/S (IDUA) * Sequencing (complete) EDTA blood / DNA 2-3 weeks Mucopolysaccharidosis 2 (IDS) * Sequencing (complete) & MLPA EDTA blood 2-3 weeks Mucopolysaccharidosis 3A[diagenom.de] […] type II; MPSII Mucopolysaccharidosis type 2, attenuated form (MPS) ORPHA217093 E76.1 Hunter syndrome type B Iduronate 2-sulfatase deficiency type B Mucopolysaccharidosis[catalogue.rd-connect.eu] ) EDTA blood / DNA 2-3 weeks Mucopolysaccharidosis 7 (GUSB) * Sequencing (complete) EDTA blood / DNA 2-3 weeks Mucopolysaccharidosis 9 (HYAL) * Sequencing (complete) EDTA[diagenom.de]

  • Mucopolysaccharidosis 1

    2 Mucopolysaccharidosis MPS-I-H Mucopolysaccharidosis MPS-I-H/S Mucopolysaccharidosis MPS-II Mucopolysaccharidosis MPS-I-S Mucopolysaccharidosis MPS-IV-A Mucopolysaccharidosis[icd9data.com] 1 mucopolysaccharidosis Англо-русский офтальмологический словарь mucopolysaccharidosis 2 mucopolysaccharidosis Англо-русский толковый словарь генетических терминов mucopolysaccharidosis[translate.academic.ru] Mucopolysaccharidosis type II Hunter syndrome (MPS 2) is the only mucopolysaccharidosis with X-linked inheritance; therefore it occurs almost exclusively in boys with an incidence[news-medical.net]

  • Mucopolysaccharidosis 1S

    Low-cost, rapidly-developed, 3D printed in vitro corpus callosum model for mucopolysaccharidosis type I [version 2; peer review: 2 approved].[f1000research.com] Management guidelines for mucopolysaccharidosis VI. Pediatrics, 2007; 120 (2):405-18. 8. Hopwood JJ, Elliott H, Muller VJ, Saccone GT.[revistamedicina.net] Low-cost, rapidly-developed, 3D printed in vitro corpus callosum model for mucopolysaccharidosis type I [version 2; peer review: 2 approved].[f1000research.com]

  • Mucopolysaccharidosis 4

    Drugs Used to Treat Mucopolysaccharidosis Type VI The following list of medications are in some way related to, or used in the treatment of this condition.[drugs.com] IVA (Morquio A Syndrome) Indication: MPS IVA (Mucopolysaccharidosis IVA, also known as Morquio A syndrome) Investigational Therapeutic: BMN 110 Study Type: Phase 2 Goal:[biomarin.com] Diagnosing mucopolysaccharidosis IVA. J Inherit Metab Dis . 2013 Mar. 36 (2):293-307. [Medline] .[emedicine.medscape.com]

  • Familial Hypercholesterolemia

    2 Mucopolysaccharidosis, MPS-II 2 Mucopolysaccharidosis, MPS-III-A 3 Mucopolysaccharidosis, MPS-III-B 2 Mucopolysaccharidosis, MPS-III-C 3 Mucopolysaccharidosis, MPS-III-D[preventiongenetics.com] III Gamma 1 Mucopolysaccharidosis Type IX 1 Mucopolysaccharidosis Type VI 1 Mucopolysaccharidosis Type VII 2 Mucopolysaccharidosis, MPS-I-H/S 1 Mucopolysaccharidosis, MPS-I-S[preventiongenetics.com] 2 Mucopolysaccharidosis, MPS-IV-B 1 Muenke Syndrome 4 Muir-Torre Syndrome 8 Mullerian Aplasia And Hyperandrogenism 6 Multiple Carboxylase Deficiency, Juvenile Onset 1 Multiple[preventiongenetics.com]

  • Mucopolysaccharidosis 3

    2 Mucopolysaccharidosis MPS-I-H Mucopolysaccharidosis MPS-I-H/S Mucopolysaccharidosis MPS-II Mucopolysaccharidosis MPS-I-S Mucopolysaccharidosis MPS-IV-A Mucopolysaccharidosis[icd9data.com] Enrollment in Phase 3 Study of Recombinant Human Beta-Glucuronidase in Mucopolysaccharidosis Type 7 (link) Ultragenyx Announces Positive 36-Week Data From Phase 1/2 Study[ultragenyx.com] Select Answer to see Preferred Response PREFERRED RESPONSE 5 (OBQ09.23) Atlantoaxial instability due to hypoplasia of the odontoid is most commonly seen in which type of mucopolysaccharidosis[orthobullets.com]

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