Lysosomal Storage Disorders Screen Interpretive Algorithm

Lysosomal Storage Disorders Screen Interpretive Algorithm

Lysosomal Storage Disorders Screen Interpretive Algorithm LSDS / Lysosomal Storage Disorders Screen, Random, Urine Testing includes: ■ Mucopolysaccharides (MPS): – Dermatan sulfate (DS) – Heparan sulfate (HS) – Keratan sulfate (KS) – Chondroitin 6-sulfate (CS) ■ Oligosaccharides (OLIGO) ■ Ceramide trihexosides (CT) ■ Sulfatides (S) ■ OLIGO: Characteristic profile ■ OLIGO: MLII/III profile ■ S: Abnormal ■ CT and S: Abnormal ■ CT: Abnormal ■ MPS and S: Abnormal ■ MPS: Abnormal ■ MPS: Abnormal ■ CT, MPS and S: Normal ■ CT, MPS and S: ■ CT, MPS and OLIGO: ■ MPS and OLIGO: ■ MPS, OLIGO and S: ■ CT and OLIGO: Normal ■ OLIGO: Characteristic profile ■ CT and S: Normal Normal/abnormal Normal Normal Normal ■ CT and S: Normal ■ OLIGO: Normal/ abnormal One of the following: Mucolipidosis II/III Metachromatic Prosaposin/SaposinB Fabry Disease Multiple sulfatase ■ α-Mannosidosis leukodystrophy (MLD) deficiency deficiency (MSD) ■ β-Mannosidosis ■ Pompe disease ■ Sandhoff disease ■ Schindler disease ■ Sialidosis ■ Elevated KS ■ Elevated KS ■ Elevated KS ■ Elevated KS ■ Elevated KS and CS ■ Galactosialidosis* ■ OLIGO: MPS ■ OLIGO: GM1 ■ OLIGO: α-Fucosidosis ■ OLIGO: Galactosialidosis ■ OLIGO: MPS IVA profile ■ α-Fucosidosis* IVB profile gangliosidosis profile profile profile ■ Mucolipidosis II/III* ■ GM1 gangliosidosis* ■ Morquio A & B* ■ NGYL1 deficiency MPS IVB GM1 gangliosidosis -Fucosidosis Galactosialidosis MPS IVA ■ MOGS-CDG (Congenital α Disorder of Glycosylation-IIb) ■ Elevated DS and HS ■ Elevated DS ■ Elevated HS ■ Elevated DS, HS, CS ■ OLIGO: Profile may ■ OLIGO: Profile may suggest MPS suggest MPS *These conditions may also have elevated MPS Interpretation of all results will include recommendations MPS I or MPS II MPS VI MPS III A, B, C, D MPS VII for confirmatory testing as needed. For confirmatory testing: See Lysosomal Storage Disorders Diagnostic Algorithm, Part 1 for MPS I, II, III, IV, VI and VII, GM1 gangliosidosis, α-fucosidosis and galactosialidosis See Lysosomal Storage Disorders Diagnostic Algorithm, Part 2 for all other disorders © Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. 03/2020.

View Full Text

Details

  • File Type
    pdf
  • Upload Time
    -
  • Content Languages
    English
  • Upload User
    Anonymous/Not logged-in
  • File Pages
    1 Page
  • File Size
    -

Download

Channel Download Status
Express Download Enable

Copyright

We respect the copyrights and intellectual property rights of all users. All uploaded documents are either original works of the uploader or authorized works of the rightful owners.

  • Not to be reproduced or distributed without explicit permission.
  • Not used for commercial purposes outside of approved use cases.
  • Not used to infringe on the rights of the original creators.
  • If you believe any content infringes your copyright, please contact us immediately.

Support

For help with questions, suggestions, or problems, please contact us