ETIMOLOGI SAKA TEMBUNG THALASSAEMIA
New Latin, from Greek thalassa sea + -aemia, from it being esp prevalent round the eastern Mediterranean Sea.
APA TEGESÉ THALASSAEMIA ING BASA INGGRIS?
Thalassemia
Thalassemia minangka bentuk kelainan getih resesif autosomal sing diwiwiti ing wilayah Mediterania. Ing talasemia, kelainan kasebut disebabake kelemahane lan karusakane sel getih abang. Thalassemia disebabake dening gen utawa varian sing ora ana sing bisa nyebabake awak dadi hemoglobin. Hemoglobin minangka protèin sel getih abang sing nggawa oksigen. Wong talasemia nyebabake hemoglobin kurang lan duwe sèl getih abang sing luwih sithik tinimbang normal, sing ngasilake anemia entheng utawa abot. Thalassemia bakal muncul minangka anemia microcytic. Thalassemia bisa nimbulaké komplikasi sing ketara, kalebu keluwihan wesi, cacat balung lan penyakit kardiovaskuler. Nanging penyakit sing diwarisake saka sel getih abang sing padha uga menehi perlindungan saka malaria, sing umum ana ing wilayah sing umum. Keuntungan kelangsungan hidup selektif pembawa mungkin tanggung jawab untuk terus mutasi ing populasi. Ing babagan kasebut, macem-macem talasemias mirip karo kelainan genetik liyane sing ngganggu hemoglobin, penyakit sel sabit.
Definisi saka thalassaemia ing bausastra Basa Inggris
Definisi talasemia sajrone kamus iku minangka penyakit herediter, umum ing pirang-pirang negara, akibat saka cacat ing sintesis hemoglobin pigmen getih abang. Uga disebut: Anemia Cooley.
BUKU BASA INGGRIS KAKAIT KARO «THALASSAEMIA»
Temukaké kagunané saka
thalassaemia ing pilihan bibliografi iki. Buku kang kakait dening
thalassaemia lan pethikan cekak kang padha kanggo nyediyakaké panggunané ing sastra Basa Inggris.
1
Thalassaemia: The Biography
Written by Sir David Weatherall, an expert in molecular medicine and the founder of the Institute of Molecular Medicine in Oxford, this tells the story of early reports of the disease, historical accounts, the identification of the disease ...
2
The
Thalassaemia Syndromes
In the new edition of this successful and authoritative book, the thalassaemias are reviewed in detail with respect to their clinical features, cellular pathology, molecular genetics, prevention and treatment.
David J. Weatherall, J. B. Clegg,
2008
3
Ethnicity and screening for sickle cell/
thalassaemia: ...
This book considers screening policies for sickle cell and thalassemia.
These genetic disorders of haemoglobin synthesis are classified by whether the
α-globin chain (α-thalassaemia) or β-globin chain (β-thalassaemia) production is
defective. The carrier state protects against falciparum malaria, explaining the ...
5
Essential Haematology, Includes Desktop Edition
The success rate (long-term thalassaemia major-free survival) is over 80–90% in
well-chelated younger patients without liver fibrosis or hepatomegaly. A human
leucocyte antigen (HLA) matching sibling (or rarely other family member or ...
Victor Hoffbrand, Paul Moss,
2011
6
Postgraduate Haematology
Haemoglobin electrophoresis shows a preponderance of HbC. The diagnosis is
confirmed by finding the HbC trait in one parent and the β thalassaemia trait in
the other. HbE/β thalassaemia This the commonest severe form of thalassaemia
in ...
A. Victor Hoffbrand, Daniel Catovsky, Edward G. D. Tuddenham,
2011
7
ABC of Clinical Haematology
αο Thalassaemia α+ Thalassaemia X HbH disease Hb H αο Thalassaemia α+
Thalassaemia Normal Figure 3.5 Inheritance of Hb disease (open boxes
represent normal α globin genes and red boxes deleted α globin genes). Normal
α2γ2 ...
8
Topics in Pathology for Hong Kong: Student Resistance to ...
In thalassaemia owing to defects in the Cl globin genes (a thalassaemia) or B
globin genes {Il thalassaemia}, imbalanced globin chain synthesis occurs.
Depending on the severity of the genetic lesions, the person with thalassaemia
can have ...
Faith C.S. Ho, P.C. Wu,
1995
9
Variant Haemoglobins: A Guide to Identification
FOUR THE THALASSAEMIAS AND RELATED CONDITIONS The term
thalassaemia covers a group of disorders of globin chain synthesis in which a
reduced rate of synthesis of one or more of the globin chains leads to a reduced
rate of ...
Barbara J. Bain, Barbara Wild, Adrian Stephens,
2011
b) Inherited Defects in the Structure and Rate of Synthesis ofHb Some of the
abnormalities such as HbE//3-thalassaemia disease will be considered here and
others like HbS//3-thalassaemia will be reviewed in another section of this
chapter.
BABAGAN WARTA KANG NGLEBOKAKÉ ARAN «THALASSAEMIA»
Weruhi yèn pawarta nasional lan internasional wis ngomongaké lan kepriyé aran
thalassaemia digunakaké ing babagan warta iki.
The report made many alarming revelations, besides identifying …
LAHORE: The Punjab Thalassaemia Prevention Programme (PTPP) has been found lacking in various vital areas concerning children suffering from the ... «DAWN.com, Jun 15»
World Thalassaemia Day: 'National policy needed for prevention'
She explained that there are around 100,000 patients of thalassaemia major from an estimated total of 10 million carriers and about 6,000 new cases surface ... «The Express Tribune, Mei 15»
Delhi Hospitals to Sensitise Staff and Public on Thalassaemia
Delhi Hospitals to start a programme in order to create awareness, sensitisation and trainings on Thalassaemia. (Representational Image, Thinkstock) ... «NDTV, Mei 15»
There are around 100000 children with thalassaemia in Pakistan on …
KARACHI: Experts at a press briefing on Thursday said thalassaemia was spreading in Pakistan at an alarmingly rate, which could be gauged from the fact that ... «DAWN.com, Apr 15»
Prenatal diagnosis and Thalassaemia
Thalassaemia is the most common congenital disorder in Bangladesh. Treatment facilities are limited due to high cost of drugs and limited availability of blood ... «The Daily Star, Mar 15»
Thalassaemia patients with HIV, or not
Earlier this month news items appeared in many newspapers that ten or more children suffering from Thalassaemia Major (an inherited blood disorder that ... «The News on Sunday, Des 14»
New screening method for thalassaemia patients in Abu Dhabi
According to the Emirates Thalassaemia Society, one in 12 Emiratis is a carrier for thalassaemia, which is a group of inherited blood disorders where the ... «The National, Des 14»
Thalassaemia cases on the rise due to lack of prevention centres
KARACHI: Haematologist Dr Saqib Hussain Ansari on Saturday revealed thalassaemia cases had gone up sharply in a decade in Sindh due to non-existence of ... «Daily Times, Des 14»
Thalassaemia-AIDS controversy: Two-member committee formed to …
ISLAMABAD: The government has constituted a two-member team to look into reports of 10 thalassaemic children testing positive for HIV after getting blood ... «The Express Tribune, Des 14»
Thalassaemia all but eradicated in Dubai
It is caused by the deterioration and destruction of red blood cells. There are different types of thalassaemia: there may be no symptoms, or it may be a serious, ... «The National, Sep 14»