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Nonimmune fetal hydrops and lysosomal storage disease: the finding of vacuolated lymphocytes in ascitic fluid in two cases
dc.contributor.authorDugan, R. B.en_US
dc.contributor.authorPletneva, M. A.en_US
dc.contributor.authorSalari, K.en_US
dc.contributor.authorBerman, D. R.en_US
dc.contributor.authorTreadwell, M. C.en_US
dc.date.accessioned2014-02-11T17:57:00Z
dc.date.available2015-04-01T19:59:06Zen_US
dc.date.issued2014-02en_US
dc.identifier.citationDugan, R. B.; Pletneva, M. A.; Salari, K.; Berman, D. R.; Treadwell, M. C. (2014). "Nonimmune fetal hydrops and lysosomal storage disease: the finding of vacuolated lymphocytes in ascitic fluid in two cases." Prenatal Diagnosis 34(2): 199-201.en_US
dc.identifier.issn0197-3851en_US
dc.identifier.issn1097-0223en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/102650
dc.publisherSpringeren_US
dc.publisherWiley Periodicals, Inc.en_US
dc.titleNonimmune fetal hydrops and lysosomal storage disease: the finding of vacuolated lymphocytes in ascitic fluid in two casesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbsecondlevelObstetrics and Gynecologyen_US
dc.subject.hlbsecondlevelRadiologyen_US
dc.subject.hlbsecondlevelWomen's and Gender Studiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelHumanitiesen_US
dc.subject.hlbtoplevelSocial Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/102650/1/pd4274.pdf
dc.identifier.doi10.1002/pd.4274en_US
dc.identifier.sourcePrenatal Diagnosisen_US
dc.identifier.citedreferenceBellini C, Hennekam RCM, Bonioli E. A diagnostic flow chart for non‐immune hydrops fetalis. Am J Med Genet Part A 2009; 149A: 852 – 3.en_US
dc.identifier.citedreferenceKooper AJA, Janssens PMW, de Groot ANJA, et al. Lysosomal storage diseases in non‐immune hydrops fetalis pregnancies. Clin Chim Acta 2006; 371: 176 – 82.en_US
dc.identifier.citedreferenceGort L, Granell MR, Fernandez G, et al. Fast protocol for the diagnosis of lysosomal diseases in nonimmune hydrops fetalis. Prenat Diagn 2012; 32: 1139 – 42.en_US
dc.identifier.citedreferenceFroissart R, Cheillan D, Bouvier R, et al. Clinical, morphological, and molecular aspects of sialic acid storage disease manifesting in utero. J Med Genet 2005; 42: 829 – 36.en_US
dc.identifier.citedreferenceBaldassarre G, Mussa A, Dotta A, et al. Prenatal features of Noonan syndrome: prevalence and prognostic value. Prenat Diagn 2011; 31: 949 – 54.en_US
dc.identifier.citedreferenceBenirschke K, Burton GJ, Baergen RN. Pathology of Human Placenta. Berlin: Springer, 2012.en_US
dc.identifier.citedreferenceAnderson G, Smith VV, Malone M, Sebire NJ. Blood film examination for vacuolated lymphocytes in the diagnosis of metabolic disorders; retrospective experience of more than 2500 cases from a single centre. J Clin Pathol 2005; 58: 1305 – 10.en_US
dc.identifier.citedreferenceSergi C, Beedgen B, Kopitz MB, et al. Refractory congenital ascites as a manifestation of neonatal sialidosis: clinical, biochemical and morphological studies in a newborn Syrian male infant. Am J Perinatol 1999; 16 ( 3 ): 133 – 41.en_US
dc.identifier.citedreferenceHann IM, Gibson BES, Letsky EA. Fetal and Neonatal Haematology ( 1st edn ), London: Bailliere Tindall, 1991.en_US
dc.identifier.citedreferenceVenkat‐Raman N, Sebire MJ, Murphy KW. Recurrent fetal hydrops due to mucopolysaccharidosis type VII. Fetal Diagn Ther 2006; 21: 250 – 4.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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