amyloidosis__familial__test_algorithm.pdf
12/2022© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. Amyloidosis (Familial) Test Algorithm* *Interpretive report provided for all tests in this algorithm. Clinical findings suggestive of familial...
Heme_Biosynthetic_Pathway.indd
08/2016© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. Porphobilinogen Succinyl Co-enzyme A Uroporphyrinogen I Uroporphyrinogen III Heptacarboxylporphyrinogen I Heptacarboxylporphyrinogen...
ganglioside_antibody_panel_algorithm.pdf
08/2024© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. Ganglioside Antibody Panel Algorithm IgG Monosialo GM1 titer is performed IgM Monosialo GM1 titer is performed IgG Disialo GD1b titer is...
helicobacter_pylori_diagnostic_algorithm.pdf
≥60 years old; OR Alarming signs and symptoms: ■ Family history of proximal gastrointestinal cancer ■ Previous malignancy of the esophagus or stomach ■ Unexplained iron-deficiency anemia ■ Palpable mass or lymphadenopathy ■ Melena ■...
cyp2d6_comprehensive_cascade_testing_algorithm.pdf
01/2024© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. CYP2D6 Comprehensive Cascade Testing Algorithm* *Additional testing is performed to derive as accurate a phenotype as possible. AAlways...
hyperoxaluria_diagnostic_algorithm.pdf
10/2024© Mayo Foundation for Medical Education and Research (MFMER). All rights reserved. Adapted from “The Primary Hyperoxalurias: An Algorithm for Diagnosis,” American Journal of Nephrology 2005;25:154-160. By permission S. Karger AG,...
MCL Whole Exome Sequencing Ordering Checklist MC1235222
MCL Exome Sequencing Ordering Checklist Complete print Exome Sequencing Ordering Checklist Reset Form Instructions Select box test requested
MCL Hemophilia A Patient Information MC1235191
MCL Hemophilia Patient Information Complete print Reset Form Hemophilia Patient Information accurate interpretation reporting genetic results contingent
MCL CYP21A2 Gene Testing for Congenital Adrenal Hyperplasia Patient Information MC1235164
MCL CYP21A2 Gene Testing Congenital Adrenal Hyperplasia Patient Information Complete print CYP21A2 Gene Testing Congenital Adrenal Hyperplasia Patient Information Reset Form Instructions Accurate interpretation reporting
wilson_disease_testing_algorithm.pdf
■ Neurological or psychiatric symptoms ± liver disease ■ Unexplained liver disease (elevated AST, ALT) ■ Normal CP and/or serum Cu ■ Normal 24-hour urine Cu ■ Normal liver function tests ■ K-F ring absent Age ≥15 years Disease-causing...