A Patient With Atypical Multiple Sulfatase Deficiency

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• 作者：Chandrabhaga Miskin ; MD^a ; ^b ; Joseph J. Melvin ; DO^a ; ^b ; Agustin Legido ; MD ; PhD ; MBA^a ; ^b ; David A. Wenger ; PhD^c ; Sue Moyer Harasink ; MS ; CGC^a ; ^b ; Divya S. Khurana ; MD^a ; ^b ; ^{divya.khurana@drexelmed.edu" class="auth_mail" title="E-mail the corresponding author}
• 关键词：multiple sulfatase deficiency ; leukodystrophy ; neurological regression
• 刊名：Pediatric Neurology
• 出版年：2016
• 出版时间：April 2016
• 年：2016
• 卷：57
• 期：Complete
• 页码：98-100
• 全文大小：398 K

文摘

Multiple sulfatase deficiency is an autosomal recessive lysosomal storage disorder characterized by the absence of several sulfatases and resulting from mutations in the gene encoding the human C (alpha)-formylglycine-generating enzyme. There have been a variety of biochemical and clinical presentations reported in this disorder.

Patient Description

We present a 4-year-old girl with clinical findings of microcephaly, spondylolisthesis and neurological regression without ichthyosis, coarse facies, and organomegaly.

Results

The child's magnetic resonance imaging demonstrated confluent white matter abnormalities involving the periventricular and deep cerebral white matter with the U-fibers relatively spared. Biochemical testing showing low arylsulfatase A levels were initially thought to be consistent with a diagnosis of metachromatic leukodystrophy. The diagnosis of multiple sulfatase deficiency was pursued when genetic testing for metachromatic leukodystrophy was negative.

Conclusion

This child illustrates the clinical heterogeneity of multiple sulfatase deficiency and that this disorder can occur without the classic clinical features.