anemia/ödem

Länken sparas på Urklipp

Välj sorteringstyp

Sida 1 från 1796 resultat

Middle cerebral artery Doppler for the prediction of fetal anaemia in cases without hydrops: a practical approach.

Endast registrerade användare kan översätta artiklar

Logga in Bli medlem

The aim of this study was to assess the value of the middle cerebral artery (MCA) Doppler time-averaged mean velocity (TAMV) for the prediction of fetal anaemia in at-risk cases without ultrasound evidence of hydrops. The study included 35 pregnant women with non-hydropic fetuses and with known red

[Manifestation of intolerance to cow's milk protein in mucoviscidosis with the symptom triad of hypoproteinemia, edema and anemia].

Endast registrerade användare kan översätta artiklar

Logga in Bli medlem

The symptom complex--hypoproteinemia, edema and anemia--occurs in approximately 5 percent of CF-patients during the first 6 months of life. Since milk is the only nutritional source in this age group, a hypocaloric nutrition respectively marginaly low protein intake may contribute to these symptoms

Recurring mutations in RPL15 are linked to hydrops fetalis and treatment independence in Diamond-Blackfan anemia.

Endast registrerade användare kan översätta artiklar

Logga in Bli medlem

Diamond-Blackfan anemia (DBA) is a rare inherited bone marrow failure disorder linked predominantly to ribosomal protein gene mutations. Here the European DBA consortium reports novel mutations identified in the RPL15 gene in 6 unrelated individuals diagnosed with DBA. Although point mutations have

A severe transfusion-dependent congenital dyserythropoietic anaemia presenting as hydrops fetalis.

Endast registrerade användare kan översätta artiklar

Logga in Bli medlem

We describe a case of congenital dyserythropoietic anaemia (CDA) presenting at week 20 of pregnancy with hydrops fetalis and very severe anaemia. Fetal blood examination showed marked erythroblastosis with morphologic alterations while the basic haematological and biochemical tests were in the

[Giant hemangioma of the placenta as a cause of life-threatening anemia in the newborn infant with hydrops congenitum].

Endast registrerade användare kan översätta artiklar

Logga in Bli medlem

A premature infant (33.-34. gestational week) delivered by caesarean section suffered from congenital hydrops and severe anaemia (7,2 g/dl) with pronounced marks of erythroblastosis; its placenta contained a haemangioma of 750 gs. A gigant haemangioma is extremely rare and can lead to a

Fetal hydrops and middle cerebral artery Doppler in prediction degree of fetal anemia and the best timing for therapy.

Endast registrerade användare kan översätta artiklar

Logga in Bli medlem

OBJECTIVE To determine the role of fetal multiples of the median of middle cerebral artery peak systolic velocity (MoM MCA-PSV), in predicting the degree of fetal anemia for determination of the best timing for the second intrauterine intravascular transfusion (IUIVT) in hydropic fetuses with Rh

Perinatal Lethal Gaucher Disease due to RecNcil Recombinant Mutation in the GBA Gene Presenting with Hydrops Fetalis and Severe Congenital Anemia.

Endast registrerade användare kan översätta artiklar

Logga in Bli medlem

A 35-year-old woman presented at 27-week gestation with hypertension and pedal edema. Antenatal scan showed hydrops fetalis and growth restriction. Cordocentesis showed severe fetal anemia. This was treated with multiple in utero blood transfusions with no clinically significant improvement and

Intrauterine aplastic anemia and fetal hydrops: a case report.

Endast registrerade användare kan översätta artiklar

Logga in Bli medlem

Fetal hydrops developed in the 8-day interval between two ultrasonographic examinations of a pregnant woman who had presented with a revealed placental abruption. Chronic ulcerative colitis had been treated with oral prednisone and sulfasalazine until the second month of pregnancy and then with

Hydrops fetalis-associated congenital dyserythropoietic anemia treated with intrauterine transfusions and bone marrow transplantation.

Endast registrerade användare kan översätta artiklar

Logga in Bli medlem

Hydrops fetalis is rarely caused by congenital dyserythropoietic anemia (CDA). We report a patient with hydrops fetalis as a result of severe anemia. This patient needed intrauterine transfusions from 21 weeks of gestation until birth. The hematologic study showed an atypical CDA (hydrops

Hydrops in fetal sheep from rapid induction of anemia.

Endast registrerade användare kan översätta artiklar

Logga in Bli medlem

We operated on 14 singleton fetal sheep at 126 +/- 3 d gestation and produced nonimmune anemia in 12 of them to study the mechanisms responsible for hydrops. Two fetuses served as controls. Partial exchange transfusions were performed daily to lower the hematocrit while we measured arterial blood

Absent thumb, immune disorder, and congenital anemia presenting with hydrops fetalis.

Endast registrerade användare kan översätta artiklar

Logga in Bli medlem

A patient is described who presented with severe congenital anemia, hydrops fetalis, immune disorder, and absent thumbs. No toxic, infectious, or metabolic cause was found to explain these symptoms. Immunologic and cytogenetic studies excluded several syndromes that combine radial ray anomalies with

Clinical presentation and outcome of 20 fetuses with parvovirus B19 infection complicated by severe anemia and/or fetal hydrops.

Endast registrerade användare kan översätta artiklar

Logga in Bli medlem

OBJECTIVE The aim of this study was to assess the prognosis of parvovirus B19 infection with severely anemic and/or hydropic fetuses according to initial ultrasound and biological criteria. METHODS Retrospective study of 20 cases of congenital parvovirus B19-proven infection (positive PCR)

Neonatal hemochromatosis: a rare cause of nonimmune hydrops fetalis and fetal anemia.

Endast registrerade användare kan översätta artiklar

Logga in Bli medlem

Neonatal hemochromatosis is a rare inherited disorder of iron metabolism in which various tissues contain excessive amounts of iron. Only in a very few cases in which the disease is associated with fetal nonimmune hydrops is there the possibility for prenatal diagnosis. We present a case of fetal

Mesalazine as a cause of fetal anemia and hydrops fetalis: A case report.

Endast registrerade användare kan översätta artiklar

Logga in Bli medlem

BACKGROUND Mesalazine and its prodrug sulfasalazine are both used for inflammatory bowel disease. Sulfasalazine has been associated with hematological side-effects such as aplastic and hemolytic anemia in patients, but also in fetuses after intrauterine exposure. To our knowledge, we describe the

Noninvasive diagnosis of anemia in hydrops fetalis with the use of middle cerebral artery Doppler velocity.

Endast registrerade användare kan översätta artiklar

Logga in Bli medlem

OBJECTIVE The purpose of this study was to assess the value of the middle cerebral artery time-averaged mean velocity for the detection of anemia as the cause of fetal hydrops. METHODS We examined 17 pregnant women with fetuses with hydrops (with ascites as the main component of hydrops) and who

Tidigare
1
2
3
4
5
6
...
119
120
Nästa

Gå med på vår
facebook-sida

Herbal & Natural Medicine

Den mest kompletta databasen med medicinska örter som stöds av vetenskapen

Fungerar på 55 språk
Växtbaserade botemedel som stöds av vetenskap
Örter igenkänning av bild
Interaktiv GPS-karta - märka örter på plats (kommer snart)
Läs vetenskapliga publikationer relaterade till din sökning
Sök efter medicinska örter efter deras effekter
Organisera dina intressen och håll dig uppdaterad med nyheterna, kliniska prövningar och patent

Skriv ett symptom eller en sjukdom och läs om örter som kan hjälpa, skriv en ört och se sjukdomar och symtom den används mot.
* All information baseras på publicerad vetenskaplig forskning