इंग्रजी शब्दकोशामध्ये "Tay-Sachs disease" याचा अर्थ

शब्दाची व्युत्पत्ती TAY-SACHS DISEASE

Named after W. Tay (1843–1927), British physician, and B. Sachs (1858–1944), US neurologist.

व्युत्पत्ती शब्दांच्या मुळाचा अभ्यास आणि संरचना आणि महत्त्व यांमधील बदलांचा अभ्यास आहे.

इंग्रजी मध्ये TAY-SACHS DISEASE चा उच्चार

Tay-Sachs disease  [ˌteɪˈsæks]

इंग्रजी मध्ये TAY-SACHS DISEASE म्हणजे काय?

Tay-Sachs रोग

Tay–Sachs disease

Tay-Sachs रोग एक दुर्मिळ स्वयंसिओल अप्रकट आनुवंशिक डिसऑर्डर आहे. त्याच्या सर्वात सामान्य प्रकारात, त्यास सहा महिन्यांपूर्वी सुरू होणा-या मज्जातची पेशी आणि मानसिक आणि शारीरिक क्षमतेचे प्रगतीशील बिघाड होते आणि सामान्यत: चार वर्षांच्या वयापर्यंत मृत्यु होते. मेंदूच्या मज्जातंतू पेशींमध्ये गँगलीसाइड म्हणून ओळखले जाणारे सेल झिल्लीचे घटक हानिकारक प्रमाणात साठतात तेव्हा ही रोग उद्भवते आणि अखेरीस ते पेशींच्या अकाली मृत्यूला लागतात. गँगलीसाइड हे स्पिंगोलिपिडचे एक रूप आहे, जे टि-स्सस रोग स्पीिंगोलीपिडोस चे सदस्य करते. कोणतीही ज्ञात उपचार किंवा उपचार नाही. 18 9 4 मध्ये प्रथम डोळ्याच्या डोळ्यांच्या डोळ्यांच्या डोळ्यांच्या डोळयावर लालसा दिसला आणि माउंट सिनाई हॉस्पिटल, न्यू यॉर्कच्या अमेरिकन न्यूरोलॉजिस्ट बर्नार्ड सॅक्सच्या नंतर 18 9 7 मध्ये याचे वर्णन करण्यात आले. Tay-Sachs रोग आणि पूर्व युरोपियन ऍशकेनाझी यहूदी लोकसंख्या मध्ये वाढ रोग प्रादुर्भाव नोंद. 20 व्या शतकाच्या उत्तरार्धात संशोधनाने सिद्ध केले की, Tay-Sachs रोग गुणसूत्र 15 वर HEXA जीनमधील आनुवंशिक उत्परिवर्तनामुळे होतो.

Tay–Sachs disease is a rare autosomal recessive genetic disorder. In its most common variant, it causes a progressive deterioration of nerve cells and of mental and physical abilities that begins around six months of age and usually results in death by the age of four. The disease occurs when harmful quantities of cell membrane components known as gangliosides accumulate in the brain's nerve cells, eventually leading to the premature death of the cells. A ganglioside is a form of sphingolipid, which makes Tay–Sachs disease a member of the sphingolipidoses. There is no known cure or treatment. The disease is named after the British ophthalmologist Waren Tay, who in 1881 first described a symptomatic red spot on the retina of the eye, and after the American neurologist Bernard Sachs of Mount Sinai Hospital, New York, who described in 1887 the cellular changes of Tay–Sachs disease and noted an increased disease prevalence in the Eastern European Ashkenazi Jewish population. Research in the late 20th century demonstrated that Tay–Sachs disease is caused by a genetic mutation in the HEXA gene on chromosome 15.

इंग्रजी शब्दकोशातील Tay-Sachs disease व्याख्या

शब्दकोषातील टे-स्सस रोगाची व्याख्या ही एक वारसा असणारी विकार आहे, जो दोषपूर्ण अप्रभावीय जीनमुळे उद्भवते, ज्यामध्ये मेंदूमध्ये लिपिड जमतात ज्यामुळे मानसिक मंद होणे आणि अंधत्व निर्माण होते. हे अशकेनाझी ज्यू मध्ये मुख्यतः उद्भवते

TAY-SACHS DISEASE चे भाषांतर

आमच्या इंग्रजी बहुभाषी भाषांतरकर्त्यासह Tay-Sachs disease चे 25 भाषांमधील भाषांतर शोधा.

या विभागात सादर केलेल्या इंग्रजी चा Tay-Sachs disease इतर भाषेतली भाषांतरे स्वयंचलित सांख्यिकीय भाषांतराद्वारे प्राप्त झाली आहेत; जिथे आवश्यक भाषांतर युनिट इंग्रजी चा «Tay-Sachs disease» हा शब्द आहे.

• भाषांतरकर्ता इंग्रजी - चीनी: 泰萨二氏病
• भाषांतरकर्ता इंग्रजी - स्पॅनिश: La enfermedad de Tay - Sachs
• इंग्रजी: Tay-Sachs disease
• भाषांतरकर्ता इंग्रजी - हिन्दी: तय सैक्स रोग
• भाषांतरकर्ता इंग्रजी - अरबी: مرض تاي ساكس
• भाषांतरकर्ता इंग्रजी - रशियन: Болезнь Тея-Сакса
• भाषांतरकर्ता इंग्रजी - पोर्तुगीज: A doença de Tay -Sachs
• भाषांतरकर्ता इंग्रजी - बंगाली: টায়-শ্যাস রোগ
• भाषांतरकर्ता इंग्रजी - फ्रेंच: La maladie de Tay - Sachs
• भाषांतरकर्ता इंग्रजी - मलय: Penyakit Tay-Sachs
• भाषांतरकर्ता इंग्रजी - जर्मन: Tay -Sachs-Krankheit
• भाषांतरकर्ता इंग्रजी - जपानी: テイ·サックス病
• भाषांतरकर्ता इंग्रजी - कोरियन: 테이 - 삭스 병
• भाषांतरकर्ता इंग्रजी - जावानीज: Penyakit Tay-Sachs
• भाषांतरकर्ता इंग्रजी - व्हिएतनामी: Bệnh Tay-Sachs
• भाषांतरकर्ता इंग्रजी - तमिळ: டாய் சாக்ஸ் நோய்
• भाषांतरकर्ता इंग्रजी - मराठी: Tay-Sachs रोग
• भाषांतरकर्ता इंग्रजी - तुर्की: Tay-Sachs hastalığı
• भाषांतरकर्ता इंग्रजी - इटालियन: Malattia di Tay - Sachs
• भाषांतरकर्ता इंग्रजी - पोलिश: Choroba Tay -Sachsa
• भाषांतरकर्ता इंग्रजी - युक्रेनियन: Хвороба Тея - Сакса
• भाषांतरकर्ता इंग्रजी - रोमानियन: Boala Tay - Sachs
• भाषांतरकर्ता इंग्रजी - ग्रीक: Νόσος Tay - Sachs
• भाषांतरकर्ता इंग्रजी - अफ्रिकान्स: Tay - Sachs siekte
• भाषांतरकर्ता इंग्रजी - स्वीडिश: Tay - Sachs sjukdom
• भाषांतरकर्ता इंग्रजी - नॉर्वेजियन: Tay - Sachs sykdom

«TAY-SACHS DISEASE» संबंधित इंग्रजी पुस्तके

खालील ग्रंथसूची निवडीमध्ये Tay-Sachs disease चा वापर शोधा. इंग्रजी साहित्यामध्ये वापराचा संदर्भ देण्यासाठी Tay-Sachs disease शी संबंधित पुस्तके आणि त्याचे थोडक्यात उतारे.

Tay-Sachs Disease

Tay-Sachs disease is a rare, hereditary disease that affects young children, primarily Ashkenazi Jews, French Canadians, and other isolated or self-selecting populations.

Jeri Freedman, 2009

Tay-Sachs Disease

They are written and edited by recognized leaders in the field and make this an essential series of books for anyone in the genetics field.

‎2001

Tay-Sachs Disease

Describes the history and causes of Tay-Sachs disease, and discusses the special needs and complications that can arise.

Julie Walker, 2007

NORD Guide to Rare Disorders

DEFINITION: Tay-Sachs disease (TSD) is a progressive, neurodegenerative disorder that results from a genetically determined deficiency of the enzyme hexosaminidase that causes the accumulation of GM2-ganglioside and/or other complex ...

National Organization for Rare Disorders, 2003

Neurogenetics: Methods and Protocols

Introduction Tay-Sachs disease is a severe, neurodegenerative disease fatal in childhood that is caused by deficiency of the enzyme β-hexosaminidase A (Hex A ) (1). Tay-Sachs is most common in the Ashkenazi Jewish population, with an ...

Nicholas T. Potter, 2003

The Troubled Dream of Genetic Medicine: Ethnicity and ...

In this captivating account, historians Keith Wailoo and Stephen Pemberton reveal how these diseases—fraught with ethnic and racial meanings for many Americans—became objects of biological fascination and crucibles of social debate.

Keith Wailoo, Stephen Pemberton, 2008

Patient in the Womb

the first child born to the couple died of Tay-Sachs disease. These parents have often accepted the 25 percent risk of having another affected child, only to be distressed that the second child displayed the disease. Unfortunately, then, in this  ...

Erminio Peter Volpe, 1984

Inborn Metabolic Diseases: Diagnosis and Treatment

In Tay-Sachs disease (affecting the subunit), hexosaminidase A only is deficient. In Sandhoff disease (affecting the -subunit) both hexosaminidases are inactivated. In GM2-activator deficiency, the substrate is not made available to the  ...

John Fernandes, Jean-Marie Saudubray, Georges van den Berghe, 2006

The Still Point of the Turning World

An immediate bestseller, The Still Point of the Turning World is Rapp’s memorial to her lost son and an inspiring and exquisitely moving reminder to love and live in the moment.

Emily Rapp, 2013

Epilepsy A to Z: A Concise Encyclopedia:Second Edition

Tay-Sachs disease is an autosomal recessive disorder localized to chromosome 15 (15q23-q24) that causes a genetically mediated deficit of N-acetyl- betahexosaminidase activity. It has also been referred to as GM2 gangliosidosis due to the ...

Pierre Jallon MD, Peter W. Kaplan MB, FRCP, William O. Tatum, 2009

नवीन गोष्टी ज्यामध्ये «TAY-SACHS DISEASE» ही संज्ञा समाविष्ट आहे

खालील बातम्यातील आयटमच्या संदर्भात राष्ट्रीय आणि आंतरराष्ट्रीय पत्रकार कशाबद्दल बोलले आहेत आणि Tay-Sachs disease ही संज्ञा कशी वापरली आहे ते शोधा.

Your Health: Clanton boy the only Alabama child battling rare Tay …

Against many complications of a disease that progressively destroys nerve cells in his brain ... Typically, children with Tay-Sachs disease live two to five years. «Alabama's News Leader, जुलै 15»

Daughter's Tay-Sachs disease didn't stop two dads from reaching for …

Krystie suffered and died from a rare disease, Tay-Sachs, but her life was by no means tragic. She traveled the country, from California beaches to the trading ... «Minneapolis Star Tribune, जून 15»

Well | Think Like a Doctor: Taking a Stand Solved

Tay-Sachs disease was first identified by two physicians, independently, in the 1880s. Dr. Warren Tay was an ophthalmologist in London. Dr. Bernard Sachs ... «New York Times, मे 15»

'This disease takes away everything': One family's story of Tay-Sachs

The first clue that something might be wrong with Cameron was, oddly enough, a diagnosis of Tay-Sachs disease in her cousin. Cameron had just received a ... «Boston Business Journal, फेब्रुवारी 15»

Tay-Sachs and the Irish Community

They were diagnosed with Tay-Sachs disease at the Children's Hospital of Philadelphia—27 years apart. The time in between has been filled with advances in ... «Mainline Today, फेब्रुवारी 15»

Hilton Head mother fundraises for Tay-Sachs cure

Alexis and Bill Buryk, parents of Katie and Allie Buryk who were diagnosed with late onset Tay-Sachs disease at the end of 2014, talk about finding out about ... «Hilton Head Island Packet, फेब्रुवारी 15»

Fair will offer genetic testing and disease information

The samples found Michelle, 30, was a carrier of Maple Syrup Urine Disease. ... Dana Zimmerman wanted to know: Was she a carrier of Tay-Sachs disease? «Sun Sentinel, एक 15»

Southern Lehigh students hope to spread Tay-Sachs disease …

There is no cure for Tay-Sachs, which can strike during infancy, early childhood and adolescence or early adulthood. The disease causes progressive ... «lehighvalleylive.com, नोव्हेंबर 14»

1000 New York Irish to get tested for Tay Sachs disease gene

On September 7, Tay-Sachs disease researchers from Einstein Medical Center in Philadelphia are coming to New York to conduct a study that will determine the ... «IrishCentral, ऑगस्ट 14»

Tay-Sachs screening urged for the Irish

Genetic screening in the Jewish community has been so successful that the number of babies born with Tay-Sachs disease has plummeted and attention is now ... «The Journal News | LoHud.com, ऑगस्ट 14»