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Increased urinary sulfite

MedGen UID:
338580
•Concept ID:
C1848957
•
Finding

Recent clinical studies

Diagnosis

Isolated sulfite oxidase deficiency: a founder mutation.
Mhanni AA, Greenberg CR, Spriggs EL, Agatep R, Sisk RR, Prasad C
Cold Spring Harb Mol Case Stud 2020 Dec;6(6) Epub 2020 Dec 17 doi: 10.1101/mcs.a005900. PMID: 33335014Free PMC Article

Prognosis

Isolated sulfite oxidase deficiency: a founder mutation.
Mhanni AA, Greenberg CR, Spriggs EL, Agatep R, Sisk RR, Prasad C
Cold Spring Harb Mol Case Stud 2020 Dec;6(6) Epub 2020 Dec 17 doi: 10.1101/mcs.a005900. PMID: 33335014Free PMC Article

Clinical prediction guides

Isolated sulfite oxidase deficiency: a founder mutation.
Mhanni AA, Greenberg CR, Spriggs EL, Agatep R, Sisk RR, Prasad C
Cold Spring Harb Mol Case Stud 2020 Dec;6(6) Epub 2020 Dec 17 doi: 10.1101/mcs.a005900. PMID: 33335014Free PMC Article

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