Multiple Sulfatase Deficiency (MSD; OMIM 272200) is a rare autosomal recessive inborn error of metabolism caused by mutations in the sulfatase modifying factor 1 gene, encoding the formylglycine-generating enzyme (FGE), and resulting in tissue accumulation of sulfatides, sulphated glycosaminoglycans, sphingolipids and steroid sulfates. Less than 50 cases have been published so far. We report a new case of MSD presenting in the newborn period with hypotonia, apnoea, cyanosis and rolling eyes, hepato-splenomegaly and deafness. This patient was compound heterozygous for two so far undescribed SUMF1 mutations

Multiple sulfatase deficiency with neonatal manifestation / Garavelli, L., Santoro, L., Iori, A., Gargano, G., Braibanti, S., Pedori, S., Melli, N., Frattini, D., Zampini, L., Galeazzi, T., Padella, L., Pepe, S., Wischmeijer, A., Rosato, S., Ivanovski, I., Iughetti, L., Gelmini, C., Bernasconi, S., Superti Furga, A., Ballabio, A., et al.. - In: THE ITALIAN JOURNAL OF PEDIATRICS. - ISSN 1824-7288. - 40:86(2014), p. 10.1186. [10.1186/PREACCEPT-1246866641374934]

Multiple sulfatase deficiency with neonatal manifestation.

BALLABIO, ANDREA;
2014

Abstract

Multiple Sulfatase Deficiency (MSD; OMIM 272200) is a rare autosomal recessive inborn error of metabolism caused by mutations in the sulfatase modifying factor 1 gene, encoding the formylglycine-generating enzyme (FGE), and resulting in tissue accumulation of sulfatides, sulphated glycosaminoglycans, sphingolipids and steroid sulfates. Less than 50 cases have been published so far. We report a new case of MSD presenting in the newborn period with hypotonia, apnoea, cyanosis and rolling eyes, hepato-splenomegaly and deafness. This patient was compound heterozygous for two so far undescribed SUMF1 mutations
2014
Multiple sulfatase deficiency with neonatal manifestation / Garavelli, L., Santoro, L., Iori, A., Gargano, G., Braibanti, S., Pedori, S., Melli, N., Frattini, D., Zampini, L., Galeazzi, T., Padella, L., Pepe, S., Wischmeijer, A., Rosato, S., Ivanovski, I., Iughetti, L., Gelmini, C., Bernasconi, S., Superti Furga, A., Ballabio, A., et al.. - In: THE ITALIAN JOURNAL OF PEDIATRICS. - ISSN 1824-7288. - 40:86(2014), p. 10.1186. [10.1186/PREACCEPT-1246866641374934]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/610876
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