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[Sickle cell anemia in perinatal placental diagnostics].

作者信息

Oppitz M, Klee A, Panitz H-G, Gonser M, Fisseler-Eckhoff A

机构信息

Institut für Pathologie und Zytologie, Dr. Horst Schmidt-Klinken, Wiesbaden, Deutschland.

出版信息

Pathologe. 2009 Jul;30(4):326-8, 330-1. doi: 10.1007/s00292-009-1137-0.

DOI:10.1007/s00292-009-1137-0
PMID:19252911
Abstract

Hereditary hemoglobinopathies should be considered as differential diagnosis when examining placental specimens for fetal growth retardation and spontaneous abortion. They can cause various macroscopic and microscopic changes in the placenta that are relevant for routine pathology examination. The importance of interdisciplinary co-operation between obstetrics and pathology to achieve optimum diagnostics and therapy planning is demonstrated using the case of a pregnant woman with heterozygous genotype and her child with homozygous genotype. Within this context, the influence of hemoglobinopathies on placental pathology and fetal development are summarized and exemplified.

摘要

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1
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本文引用的文献

1
DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease.BCL11A、HBS1L-MYB和β-珠蛋白基因座的DNA多态性与镰状细胞病中的胎儿血红蛋白水平和疼痛危象相关。
Proc Natl Acad Sci U S A. 2008 Aug 19;105(33):11869-74. doi: 10.1073/pnas.0804799105. Epub 2008 Jul 30.
2
The mechanisms of low birth weight in infants of mothers with homozygous sickle cell disease.患有纯合子镰状细胞病母亲所生婴儿低出生体重的机制。
Pediatrics. 2007 Sep;120(3):e686-93. doi: 10.1542/peds.2006-2768.
3
Sickle cell anemia in the female patient.
女性患者的镰状细胞贫血。
Obstet Gynecol Surv. 2006 May;61(5):343-52. doi: 10.1097/01.ogx.0000216976.15100.29.
4
Outcome of pregnancy in homozygous sickle cell disease.纯合子镰状细胞病的妊娠结局。
Obstet Gynecol. 2004 Jun;103(6):1278-85. doi: 10.1097/01.AOG.0000127433.23611.54.
5
Images in pathology. The placenta in sickle cell disease.病理学图像。镰状细胞病中的胎盘。
Arch Pathol Lab Med. 2000 Oct;124(10):1565. doi: 10.5858/2000-124-1565-TPISCD.