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[Fetal ascites as a manifestation of infantile sialidosis. Significance of a study of oligosaccharides in amniotic fluid].

作者信息

Guibaud P, Cottin X, Maire I, Boyer S, Guibaud S, Coicaud C, Bellon-Azzouzi C, Duvernois J P

出版信息

J Genet Hum. 1985 Sep;33(3-4):317-24.

PMID:2414397
Abstract

Non immune hydramnios and fetal ascite are demonstrated at 31 weeks gestation. There is no familial story. All etiologic investigations (repeated ultrasonographic examinations, amniocentesis) are negative. The delivered girl has a normal development. She presents a congenital ascite and edema. The diagnosis of sialidosis (mucolipidosis type I) is supported by the early finding of vacuolated lymphocytes, the excretion of oligosaccharides in the urine and, finally, the results of the study of alpha-D-neuraminidase fibroblasts and others lysosomal enzymes activities. Oligosaccharides and enzymic studies provide same results in amniotic fluid. Authors point the particular interest of amniotic fluid oligosaccharides study when the etiologic diagnosis of idiopathic fetal ascite or hydrops is to be done.

摘要

相似文献

1
[Fetal ascites as a manifestation of infantile sialidosis. Significance of a study of oligosaccharides in amniotic fluid].
J Genet Hum. 1985 Sep;33(3-4):317-24.
2
Determination of oligosaccharides and glycolipids in amniotic fluid by electrospray ionisation tandem mass spectrometry: in utero indicators of lysosomal storage diseases.通过电喷雾电离串联质谱法测定羊水中的寡糖和糖脂:溶酶体贮积病的宫内指标
Mol Genet Metab. 2004 Nov;83(3):231-8. doi: 10.1016/j.ymgme.2004.07.015.
3
[Biochemical analysis of the amniotic fluid in early amniocentesis. Importance of alpha-fetoproteins].[早期羊膜腔穿刺术中羊水的生化分析。甲胎蛋白的重要性]
Minerva Ginecol. 1980 Jun;32(6):539-44.
4
Congenital ascites as a presenting sign of lysosomal storage disease.先天性腹水作为溶酶体贮积病的首发症状
J Pediatr. 1984 Feb;104(2):225-31. doi: 10.1016/s0022-3476(84)80997-x.
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Prenatal diagnosis and management of nonimmunologic hydrops fetalis.胎儿非免疫性水肿的产前诊断与处理
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8
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9
[Alpha-fetoprotein in the amniotic fluid in pregnancies at high risk for congenital fetal defect and Rh isoimmunization].[先天性胎儿缺陷和Rh血型免疫的高危妊娠中羊水甲胎蛋白的情况]
Ann Ostet Ginecol Med Perinat. 1981 Mar-Apr;102(2):75-83.
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Elevated alpha-fetoprotein and acetylcholinesterase associated with hydrocele.与鞘膜积液相关的甲胎蛋白和乙酰胆碱酯酶升高。
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引用本文的文献

1
Sialidosis: A Review of Morphology and Molecular Biology of a Rare Pediatric Disorder.唾液酸沉积症:一种罕见儿科疾病的形态学与分子生物学综述
Diagnostics (Basel). 2018 Apr 25;8(2):29. doi: 10.3390/diagnostics8020029.
2
Lysosomal storage disorder in non-immunological hydrops fetalis (NIHF): more common than assumed? Report of four cases with transient NIHF and a review of the literature.非免疫性胎儿水肿(NIHF)中的溶酶体贮积症:比想象中更常见?4 例伴有短暂 NIHF 的病例报告及文献复习。
Orphanet J Rare Dis. 2012 Nov 8;7:86. doi: 10.1186/1750-1172-7-86.
3
Type II sialidosis: review of the clinical spectrum and identification of a new splicing defect with chitotriosidase assessment in two patients.
Ⅱ型唾液酸贮积症:临床表型综述及通过几丁质酶活性检测在两例患者中鉴定的新剪接缺陷。
J Neurol. 2009 Nov;256(11):1911-5. doi: 10.1007/s00415-009-5213-4. Epub 2009 Jul 1.
4
Lysosomal storage disorders in the newborn.新生儿溶酶体贮积症
Pediatrics. 2009 Apr;123(4):1191-207. doi: 10.1542/peds.2008-0635.