Tegesé saka "sickle-cell anaemia" ing bausastra Basa Inggris

PANGOCAP SAKA SICKLE-CELL ANAEMIA ING BASA INGGRIS

sickle-cell anaemia

APA TEGESÉ SICKLE-CELL ANAEMIA ING BASA INGGRIS?

Penyakit sel sabit

Sickle-cell disease

Penyakit sel sabit, utawa anemia sel sabit utawa drepanocytosis, yaiku kelainan getih sing ditemtokake, ditondoi dening sel getih abang sing nganggep wujud sing ora normal, kaku, lan sabit. Sickling ngurangi keluwesan sel lan nimbulaké risiko saka macem-macem komplikasi sing ngancam nyawa. Gerah iki amarga mutasi ing gén hemoglobin. Individu karo siji salinan gen mutant ngasilake campuran hemoglobin normal lan abnormal. Iki minangka conto dominasi mboten pepak. Pangarepan urip dipendhet. Ing taun 1994, ing AS, pangarep-arep urip rata-rata wong kanthi kondhisi iki kira-kira dadi 42 taun lanang lan 48 taun ing wanita, nanging dina iki, amarga manawa penyakit kasebut luwih apik, pasien bisa urip ing taun 70-an utawa luwih. Penyakit sel tumor luwih umum ing kalangan wong-wong sing leluhur manggon ing wilayah sub-saharan tropis lan sub-tropis ing ngendi malaria utawa umum. Ing endi malaria asring, ndamel alel sel sabit tunggal ndadekake kauntungan selektif - ing tembung liya, dadi heterozygote sing nguntungake.

Sickle-cell disease, or sickle-cell anaemia or drepanocytosis, is a hereditary blood disorder, characterized by red blood cells that assume an abnormal, rigid, sickle shape. Sickling decreases the cells' flexibility and results in a risk of various life-threatening complications. This sickling occurs because of a mutation in the haemoglobin gene. Individuals with one copy of the mutant gene produce a mixture of both normal and abnormal haemoglobin. This is an example of incomplete dominance. Life expectancy is shortened. In 1994, in the US, the average life expectancy of persons with this condition was estimated to be 42 years in males and 48 years in females, but today, thanks to better management of the disease, patients can live into their 70s or beyond. Sickle-cell disease occurs more commonly among people whose ancestors lived in tropical and sub-tropical sub-saharan regions where malaria is or was common. Where malaria is common, carrying a single sickle-cell allele confers a selective advantage—in other words, being a heterozygote is advantageous.

Definisi saka sickle-cell anaemia ing bausastra Basa Inggris

Definisi anemia sel sabit sajrone kamus yaiku anemia hemolisis herediter, kedadeyan ing populasi Hitam, lan disebabake dening hemoglobin mutant. Sèl-sèl getih abang dadi bentuk sabit. Iki ditondoi dening demam, nyeri weteng, jaundis, ulkus sikil, lan liya-liyane.

PERTALAN SAKA SICKLE-CELL ANAEMIA

Weruhi pertalan saka sickle-cell anaemia menyang 25 basa nganggo Basa Inggris pamertal multi basa kita.

pertalan saka sickle-cell anaemia saka Basa Inggris menyang basa liyané kang kasuguhaké ing perangan iki kajupuk saka pertalan statistik otomatis; ing ngendhi inti unit pertalan yaiku tembung «sickle-cell anaemia» ing Basa Inggris.

• Pamertal Basa Inggris - Basa Cina: 镰状细胞贫血
• Pamertal Basa Inggris - Basa Spanyol: anemia de células falciformes
• Basa Inggris: sickle-cell anaemia
• Pamertal Basa Inggris - Basa India: सिकल सेल एनीमिया
• Pamertal Basa Inggris - Basa Arab: فقر الدم المنجلي
• Pamertal Basa Inggris - Basa Rusia: серповидно - клеточная анемия
• Pamertal Basa Inggris - Basa Portugis: anemia falciforme
• Pamertal Basa Inggris - Basa Bengali: কাস্ত্র-সেল অ্যানিমিয়া
• Pamertal Basa Inggris - Basa Prancis: la drépanocytose
• Pamertal Basa Inggris - Basa Malaysia: Anemia sel sabit
• Pamertal Basa Inggris - Basa Jerman: Sichelzellenanämie
• Pamertal Basa Inggris - Basa Jepang: 鎌状赤血球貧血
• Pamertal Basa Inggris - Basa Korea: 겸상 적혈구 빈혈
• Pamertal Basa Inggris - Basa Jawa: Anemia sel sabit
• Pamertal Basa Inggris - Basa Vietnam: thiếu máu hồng cầu liềm
• Pamertal Basa Inggris - Basa Tamil: அரிசி-செல் இரத்த சோகை
• Pamertal Basa Inggris - Basa Marathi: सिकलसेल ऍनेमीया
• Pamertal Basa Inggris - Basa Turki: Orak hücreli anemi
• Pamertal Basa Inggris - Basa Italia: anemia falciforme
• Pamertal Basa Inggris - Basa Polandia: anemia sierpowata
• Pamertal Basa Inggris - Basa Ukrania: серповидно - клітинна анемія
• Pamertal Basa Inggris - Basa Romawi: siclemie
• Pamertal Basa Inggris - Basa Yunani: δρεπανοκυτταρική αναιμία
• Pamertal Basa Inggris - Basa Afrikaans: sekelselanemie
• Pamertal Basa Inggris - Basa Swedia: sickelcellanemi
• Pamertal Basa Inggris - Basa Norwegia: sigdcelleanemi

BUKU BASA INGGRIS KAKAIT KARO «SICKLE-CELL ANAEMIA»

Temukaké kagunané saka sickle-cell anaemia ing pilihan bibliografi iki. Buku kang kakait dening sickle-cell anaemia lan pethikan cekak kang padha kanggo nyediyakaké panggunané ing sastra Basa Inggris.

Focus on Sickle Cell Research

Sickle cell anaemia is a genetic disease characterized by a mutation in hemoglobin (Hb) resulting in hemoglobin polymerization and resultant cell deformation (sickling) under low oxygen conditions. The mutation is in the haemoglobin ...

Ralph L. Plasmar, 2004

New Modular Science for Gcse.

Puzzling distribution <J> In parts of Africa as many as 14% of babies bom have sickle cell anaemia and doctors were puzzled by this for many years. The map opposite provides an explanation. The map shows that the distribution of sickle cell ...

‎1997

Bio-social Issues in Health

6 Sickle Cell Anaemia: A Genetically Handicap Disease BhaskarP. Urade , Moyna Chakravarty and Sujit K. Mallick Abstract Sickle cell anemia is an autosomal recessive genetic disorder. HbS, is responsible for sickle cell disease, one of the ...

Anil Kishore Sinha, 2008

Haematology: An Illustrated Colour Text

In the first family one child is unaffected, one has sickle cell trait and one has sickle cell anaemia. In the second family one child has inherited the abnormal sickle gene and the HbC gene;this double heterozygosity leads to haemoglobin SC ...

Martin R. Howard, Peter J. Hamilton, 2008

TEXTBOOK OF BIOCHEMISTRY AND HUMAN BIOLOGY

In sickle cell anaemia and Hb C disease, the cells are deformed due to the physical changes in the haemoglobins. Haemoglobin Zurich on the other hand is an unstable haemoglobin which precipitates and leads to red cell inclusions.

G. P. TALWAR, L .M. SRIVASTAVA, 2002

District Laboratory Practice in Tropical Countries

The serious disorder sickle cell anaemia ((£l[£) is caused when a person inherits the jf gene from both parents (homozygous state). Note: The term sickle cell disease is used to describe sickle cell anaemia (HbSS) and the range of HbS related ...

Monica Cheesbrough, 2006

Sickle Cell Simply Explained

many people with sickle cell anaemia can live into middle age and beyond and have very productive lives. Indeed, it is better for the diagnosis of sickle cell anaemia to be made very early in life so that the baby can start receiving the necessary ...

Dr. John Koramoa, 2014

Haemoglobinopathy Diagnosis

... 88 hydroxycarbamide haemoglobin E/b thalassaemia, 207, 208 sickle cell anaemia, 155, 157, 159 bthalassaemia intermedia, 109 hydroxyurea seehydroxycarbamide hyperbaric oxygen therapy, carboxyhaemoglobinaemia, 243 hyperdense ...

Barbara J. Bain, 2008

New Modular Science for GCSE.: Homework book

INHERITANCE AND SELECTION a What is sickle cell anaemia? b The graphs in the previous column show the haemoglobin pattern for homozygous normal, heterozygous and homozygous sickle cell anaemia. What does this information tell ...

Ann Fullick, Patrick Fullick, Martin Stirrup, 1998

Biotechnology for Livestock Production

We've known these things for quite a long time and yet are still totally devoid of any information that allows us to be useful for a patient with sickle cell anaemia. I think that is something we must keep continually in mind. The only thing we can ...

‎1989

BABAGAN WARTA KANG NGLEBOKAKÉ ARAN «SICKLE-CELL ANAEMIA»

Weruhi yèn pawarta nasional lan internasional wis ngomongaké lan kepriyé aran sickle-cell anaemia digunakaké ing babagan warta iki.

'10% of tribals afflicted with sickle-cell anaemia'

Sickle-cell anemia is a hereditary blood disorder in which red blood cells are distorted into sickle shape at low-oxygen levels. This disorder gives rise to many ... «Times of India, Jul 15»

Jourdan Dunn on her son's sickle-cell anaemia: 'That I can't take the …

Sickle cell anaemia is a blood disorder where the red blood cells, which carry oxygen around the body, develop abnormally. The abnormal cells are also unable ... «The Independent, Apr 15»

Sickle-Cell Anaemia spreading among tribals

There is no problem if two individuals with white cards marry. The colours of the other cards are yellow and red. White card holders can marry yellow and red ... «The Hindu, Agus 14»

From catwalk queen to campaigning mum: 21-year-old supermodel …

And things didn't get any easier for the mother from Ealing after Riley was diagnosed with sickle-cell anaemia, an inherited, noncontagious blood disorder most ... «Daily Mail, Jul 12»

Sickle-cell mystery solved

Sickle-cell mystery solved ... carriers of one mutated copy of the gene that causes sickle-cell anaemia are protected from malaria. ... Enter the sickle-cell factor. «Nature.com, Nov 11»