Article
Severe isolated sulfide oxidase deficiency with a novel mutation.
The Turkish journal of pediatrics - 1 Jan 2021
Ergene Meriç, Yarar Nuriye, Öncel Elif Perihan, Sezer Taner, Çavdarlı Büşranur, Ecevit İsmail Zafer, Aydın Halil İbrahim
Abstract excerpt
BACKGROUND: Isolated sulfite oxidase deficiency (ISOD), caused by mutations in SUOX gene, is an autosomal recessive disease manifesting with early onset seizures, developmental delay, microcephaly, and spasticity. It mimics hypoxic-ischemic encephalopathy (HIE) in the neonatal period and is characterized by progressive severe neurological impairment due to accumulation of toxic metabolites. CASE: This report...
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