نتایج جستجو برای: hydrops fetalis

تعداد نتایج: 1807  

Journal: :International Journal of Reproduction, Contraception, Obstetrics and Gynecology 2014

2008
Takayoshi Hosono Kyoko Murakami Haruka Akeno Ai Nakahata Keiko Ueda Shuji Hashimoto Tomoaki Ikeda Tsuyoshi Miyashita Kuniomi Ogata Akihiko Kandori Yoshiko Sugita Tsuyohi Miyashita Keiji Tsukada

Non-immune hydrops fetalis is defined as presence of excess fluid in two or more body areas, such as the abdomen, thorax, or skin, excluding immune etiology. Major causes of non-immune fetal hydrops are fetal heart diseases and abnormal chromosome. In spite of accumulated reports of fetal magentocardiograms (FMCG) for heart diseases, FMCG for fetal hydrops of non-cardiac origin has seldom been ...

Journal: :Archives of Disease in Childhood 1983

Journal: :AJNR. American journal of neuroradiology 2016
A R Sepahdari N Vorasubin G Ishiyama A Ishiyama

Endolymphatic hydrops, the primary pathologic alteration in Menière disease, can be visualized by using delayed intravenous contrast-enhanced 3D-FLAIR MR imaging. It is not known whether MR imaging-demonstrable changes of hydrops fluctuate with disease activity or are fixed. We describe the results of baseline and posttreatment MR imaging studies in a group of subjects with Menière disease with...

Journal: :Clinical genetics 2006
A Ghalamkarpour S Morlot A Raas-Rothschild A Utkus J B Mulliken L M Boon M Vikkula

Mutations in the vascular endothelial growth factor receptor 3 gene, VEGFR3/FLT4, have been identified in a subset of families with hereditary lymphedema type I or Milroy disease (MIM 153100). Individuals carrying a VEGFR3 mutation exhibit congenital edema of the lower limbs, usually bilaterally and below the knees, sometimes associated with cellulitis, prominent veins, papillomatosis, upturned...

Journal: :Clinical and diagnostic laboratory immunology 2001
J A Jordan D Huff J A DeLoia

Human parvovirus B19 can cause congenital infection with variable morbidity and mortality in the fetus and neonate. Although much information exists on the B19-specific antibody response in pregnant women, little information is available describing the cell-mediated immune (CMI) response at the maternal-fetal interface. The focus of this study was to characterize the CMI response within placent...

Journal: :Indian journal of child health 2022

Galactosialidosis is a rare autosomal recessive lysosomal storage disorder (LSD). It results from defects in glycoprotein degradation due to mutation single gene, encoded by the protective protein cathepsin A, (CTSA), located on chromosome 20q13.12. Most cases of non-immune hydrops fetalis (NIHF) nowadays being recognized are cardiac, lymphatic dysplasia, and hematological disorders. Inborn err...

Journal: :Journal of Mahatma Gandhi University of Medical Sciences and Technology 2019

Journal: :Journal of Pediatrics, Perinatology and Child Health 2020

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