HAEMOGLOBINOPATHY SÖZCÜĞÜ İNGILIZCE DİLİNDE NE ANLAMA GELİR?
hemoglobinopati
Hemoglobinopati, hemoglobin molekülünün globin zincirlerinden birinin anormal yapısına neden olan genetik bir kusur türüdür. Hemoglobinopatiler kalıtsal tek gen bozukluklarıdır; Çoğu durumda, otozomal ortak egemen özellikler olarak kalıtsaldır. Sık görülen hemoglobinopati orak hücre hastalığıdır. Dünya nüfusunun% 7'sinin taşıyıcı olduğu, toplamda% 60 ve Afrika'da% 70'lik patolojik olduğu tahmin edilmektedir. Hemoglobinopati, Afrika, Akdeniz havzası ve Güneydoğu Asya'dan gelen etnik popülasyonlarda en yaygındır. Hemoglobinopati, globin proteinlerinin kendisinde yapısal anormallikler olduğunu gösterir. Aksine, talasemi, normal globin proteinlerinin, çoğunlukla düzenleyici genlerdeki mutasyonlar yoluyla yetersiz üretilmesine neden olur. Bununla birlikte, globin proteinlerinde anormalliklere neden olan bazı koşullar, üretimlerini de etkilediğinden, iki koşul çakışabilir. Bu nedenle, bazı hemoglobinopatiler de talasemidir, ancak çoğu yoktur. Hemoglobinopati veya talasemi veya her ikisi de, anemiye neden olabilir.
İngilizce sözlükte haemoglobinopathy sözcüğünün tanımı
Sözlükte hemoglobinopati tanımı, anormal hemoglobin ile karakterize edilen orak hücreli anemi ve talasemi de dahil olmak üzere çeşitli kalıtsal hastalıklardan herhangi biridir.
«HAEMOGLOBINOPATHY» İLE İLİŞKİLİ İNGILIZCE KİTAPLAR
haemoglobinopathy sözcüğünün kullanımını aşağıdaki kaynakça seçkisinde keşfedin.
haemoglobinopathy ile ilişkili kitaplar ve İngilizce edebiyattaki kullanımı ile ilgili bağlam sağlaması için küçük metinler.
1
Haemoglobinopathy Diagnosis
This unique book is written by Barbara Bain, a leading haematologist with a reputation for her educational prowess in the field.
2
Variant Haemoglobins: A Guide to Identification
0.0 -0.l 0.0 0.5 l .0 [.5 2.0 2.5 3.0 Time (mi-.1 United Kingdom policies for neonatal
haemoglobinopathy screening can be found in the NHS Screening Programme's
Sickle Cell and Thalassaemia Handbook for Laboratories [14]. DNA analysis ...
Barbara J. Bain, Barbara Wild, Adrian Stephens,
2011
3
The politics of sickle cell and thalassaemia
... 23, 29 haemoglobin electrophoresis, 15-16 haemoglobinopathy disorders
coping with, 72, 84-8 disability and chronic illness, 69-72 and educational
provision, 1, 71, 86, 103-5, 114 and ethnicity, 9-10 and family life, 80-4 frequency
of, 13-14 ...
Elizabeth N. Anionwu, Karl Atkin,
2001
4
Annals of the Academy of Medicine, Singapore
Most studies in various geographical regions showed that undernutrition was the
single major cause of anaemia; regardless of whether the population was urban,
suburban or rural, in the East or West (Table V).""»°"' Haemoglobinopathy was ...
5
Ethnicity and screening for sickle cell/thalassaemia: ...
They would need to explain the haemoglobinopathy-related purpose of the
question (and therefore to understand the difference between ethnic identity for
ethnic monitoring purposes and genetic ancestry for haemoglobinopathy
screening ...
Haemoglobinopathy H Haemoglobinopathy H; studies of haemoglobin synthesis
and red cell survival in haemoglobinopathy H, 124 Haemoglobinurie (bei
Favismus), v. Sialique Haemolysis, v. Anemies hémolytiques Haemophilia ...
7
Ethnicity, disability, and chronic illness
All the haemoglobinopathy counsellors were themselves from minority ethnic
groups; the majority of Asian parents were served by Asian counsellors. At a
broader level, the shortage of counsellors with skills in South Asian languages is
a ...
Waqar Ihsan-Ullah Ahmad,
2000
8
Oxford Handbook of General Practice
Chapter 19 657 Haematology and immunology Full blood count and ESR 658
Anaemia: diagnosis and initial investigation 660 Iron deficiency anaemia 662
Haemolysis and aplastic anaemia 664 Haemoglobinopathy 666 Bleeding and
clotting ...
Chantal Simon, Hazel Everitt, Francoise van Dorp,
2010
... cooling Anaemia Diagnosis: iron deficiency anaemia (dietary) Differential
diagnosis: chronic GI bleeding; coeliac; inherited haemoglobinopathy e.g. -
thalassaemia trait History Symptoms r Tiredness, lethargy and breathlessness
Differential ...
Stephen Hoole, Andrew Fry, Daniel Hodson,
2010
10
Oxford Desk Reference: Obstetrics and Gynaecology
... pregnancies previous fetal congenital abnormalities or fetal death 0 previous
fetal or neonatal anaemia or jaundice previous history of rhesus or other blood
group antibodies drug history, including recreational drug use
haemoglobinopathy ...
Sabaratnam Arulkumaran, Lesley Regan, Aris Papageorghiou,
2011
«HAEMOGLOBINOPATHY» TERİMİNİ İÇEREN HABERLER
Ulusal ve uluslararası basında konuşulanları ve
haemoglobinopathy teriminin aşağıdaki haberlerde hangi bağlamda kullanıldığını keşfedin.
Do people from the Jewish community prefer ancestry-based or pan …
... was also mentioned by Jans et al. describing attitudes of GPs and midwives regarding ancestry-based haemoglobinopathy carrier screening. «Nature.com, May 15»
Wexham Park Hosptial department selected by Department of …
The hospital's pathology department will pilot a scheme for computerised electronic requesting for patients who require haemoglobinopathy ... «Slough and Windsor Observer, Mar 15»
8% of Omanis have genes that cause blood disorders: Expert
She also added that a volunteer pre-marital blood test for haemoglobinopathy gene have been available throughout the sultanate for many ... «Muscat Daily, Şub 15»
Cocktails With — Josina Jackson
My mother is a registered nurse and for most of her career has been a haemoglobinopathy counsellor, looking after people who have sickle cell ... «Jamaica Observer, Şub 15»
Sheffield scientists make red blood cell discovery
The haemoglobinopathy diagnostics department at the Royal Hallamshire Hospital have discovered four previously undiscovered variants of ... «The Star, Şub 15»
OPD on RMRC Campus from Saturday
More than 5,000 filariasis and 2,000 haemoglobinopathy patients have been treated at the centre. The centre has conducted valuable research ... «The New Indian Express, Oca 15»
Gaining informed consent for blood transfusion
Patients who require long-term, regular transfusions - for example, those with haemoglobinopathy or haematology conditions - need to have ... «Nursing Times, Ağu 14»
Keighley health day helps raise awareness
Organiser, Janet Hall, a haemoglobinopathy counsellor with Airedale NHS Foundation Trust, said: “The aim of the event was to raise ... «Keighley News, Ara 13»
Race a factor in lack of sickle cell specialist nurses
NHS England has acknowledged there are “inequities” in access to high quality haemoglobinopathy care due to a combination of the “varied ... «Nursing Times, Eyl 13»
Queen's Birthday Honours : London's MBEs
Dr Lorna Ann Marie Bennett, clinical service manager and haemoglobinopathy counsellor, Camden and Islington Primary Care Trust. «London24, Haz 13»