نتایج جستجو برای: a cute hydrops

تعداد نتایج: 13432416  

2013
Patrick G. Gallagher

We studied a kindred in which four third-trimester fetal losses occurred, associated with severe Coombs-negative hemolytic anemia and hydrops fetalis. Postmortem examination of two infants revealed extensive extramedullary erythropoiesis. Studies of erythrocytes and erythrocyte membranes from the parents revealed abnormal erythrocyte membrane mechanical stability as well as structural and funct...

Journal: :The Journal of clinical investigation 1995
P G Gallagher S A Weed W T Tse L Benoit J S Morrow S L Marchesi N Mohandas B G Forget

We studied a kindred in which four third-trimester fetal losses occurred, associated with severe Coombs-negative hemolytic anemia and hydrops fetalis. Postmortem examination of two infants revealed extensive extramedullary erythropoiesis. Studies of erythrocytes and erythrocyte membranes from the parents revealed abnormal erythrocyte membrane mechanical stability as well as structural and funct...

2013
Behzad Fallahi Motlagh Seyed Zia Mortazavi

PURPOSE To report acute corneal hydrops following suture removal after penetrating keratoplasty (PK) in a case of pellucid marginal degeneration (PMD). CASE REPORT A young female underwent PK for corneal scarring in her left eye due to PMD; 8 months later the last sutures were removed. A few days following suture removal, the patient developed acute hydrops in the inferior aspect of the host-...

2015
Vipul Bhandari Sri Ganesh

PURPOSE To report an unusual presentation of pellucid marginal degeneration (PMD) and its management by using air injection and tension sutures. CASE REPORT We report 2 cases with a history of acute pain and loss of vision. Examination revealed hydrops at the 6-9 o'clock meridian with Descemet's membrane detachment and tear at the same area and advanced PMD in the other eye. DISCUSSION Air ...

Journal: :JPMA. The Journal of the Pakistan Medical Association 1996
F Ovali N Samanci O Ozdemir T Dagoglu

Non-immune hydrops fetalis (NIHF) in a relatively rare syndrome associated with different etiologies, usually due to chromosomal aberrations or cardiac anomalies. Human parvovirus B 19 (HPV B 19) associated intrauterine infections. NIHF and fetal loss have been reported lately. HPV B19 passes through the placenta and infects eiythroid progenitor cells with subsequent lysis, anemia and hydrops. ...

Journal: :فصلنامه علمی اکوفیزیولوژی گیاهان زراعی 0

this study was conducted to evaluate the effect of foliar micronutrients cu, mg and b on quantitative traits in two sesame crop year 1394 was performed farmer field. a split plot experiment in randomized complete block design with three replications. the main factor includes four operating cu sulfate solution, mg sulfate, b sulfate and control (water) and subplots consisted of two sesame (uniqu...

2017
Ricardo Alexandre Stock Thaís Thumé Elcio Luiz Bonamigo

BACKGROUND Keratoconus may progress to acute corneal hydrops even after cross-linking. In some cases, keratoconus progresses during pregnancy. In this report, we present a case of a patient with increased anterior stromal resistance after cross-linking that would favor nonprogression of keratoconus during pregnancy. CASE PRESENTATION We report that cross-linking is likely to have had a protec...

2015
Elisavet Fotiou Silvia Martin-Almedina Michael A Simpson Shin Lin Kristiana Gordon Glen Brice Giles Atton Iona Jeffery David C Rees Cyril Mignot Julie Vogt Tessa Homfray Michael P Snyder Stanley G Rockson Steve Jeffery Peter S Mortimer Sahar Mansour Pia Ostergaard

Generalized lymphatic dysplasia (GLD) is a rare form of primary lymphoedema characterized by a uniform, widespread lymphoedema affecting all segments of the body, with systemic involvement such as intestinal and/or pulmonary lymphangiectasia, pleural effusions, chylothoraces and/or pericardial effusions. This may present prenatally as non-immune hydrops. Here we report homozygous and compound h...

2013
Mohamed M Abdeltawwab

Ménière’s disease is a progressive idiopathic disorder that was first described by Prosper Ménière’s . The cause of the disease has not yet been clarified and remains controversial. It is, however, hypothesized that an increased amount of endolymph (endolymphatic hydrops) which causes distension of the endolymphatic sac and the endolymphatic components of the vestibular and cochlear parts may b...

2017
Maria de Lourdes Flores García Carolina de la Llata Segura Juan Carlos Cisneros Lesser Carlo Pane Pianese

The association of repeated attacks of vertigo that last for hours with a sense of aural fullness, fluctuating progressive hearing loss and tinnitus is characteristic of endolymphatic hydrops. In most cases, it is impossible to determine an etiology and a diagnosis of idiopathic endolymphatic hydrops, or Ménière’s disease, until it is established. The endolymphatic sac is thought to maintain th...

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