Maksud "neurofibromatosis" dalam kamus Corsica

SEBUTAN NEUROFIBROMATOSIS DALAM CORSICA

neurofibromatosis  [ˌnjʊərəʊˌfaɪbrəməˈtəʊsɪs]

APAKAH MAKSUD NEUROFIBROMATOSIS dalam CORSICA?

Neurofibromatosis

Neurofibromatosis

Neurofibromatosis (NF) merujuk kepada beberapa keadaan yang diwarisi yang secara klinikal dan berbeza secara genetik dan mempunyai risiko pembentukan tumor yang tinggi, terutamanya di dalam otak. Neurofibromatosis adalah gangguan dominan autosomal, yang bermaksud hanya satu salinan gen yang terjejas diperlukan untuk gangguan itu. Oleh itu, jika hanya satu orang ibu yang mempunyai neurofibromatosis, anak-anaknya mempunyai peluang 50% untuk membangunkan keadaan ini juga (jarang sekali bahawa satu orang mempunyai gen yang bermutasi dua kali, yang akan membayangkan kemungkinan 100% anak-anak mereka berkembang NF). Keparahan dalam individu terjejas boleh berbeza-beza; ini mungkin disebabkan oleh ekspresi yang berubah-ubah. Kira-kira separuh daripada kes adalah disebabkan oleh mutasi de novo dan tidak ada ahli keluarga yang terjejas lain. Ia memberi kesan kepada lelaki dan wanita sama. Di samping itu, sesetengah individu mungkin mempunyai mosaik NF, di mana beberapa tetapi tidak semua sel badan membawa mutasi itu. Neurofibromatoses adalah seperti berikut: ▪ Neurofibromatosis jenis I, di mana tisu saraf tumbuh tumor (neurofibromas) yang mungkin jinak dan boleh menyebabkan kerosakan yang serius dengan menguatkan saraf dan tisu lain.

Neurofibromatosis (NF) refers to a number of inherited conditions that are clinically and genetically distinct and carry a high risk of tumor formation, particularly in the brain. Neurofibromatosis is an autosomal dominant disorder, which means only one copy of the affected gene is needed for the disorder to develop. Therefore, if only one parent has neurofibromatosis, his or her children have a 50% chance of developing the condition as well (it is rarely the case that one person has the mutated gene twice, which would imply a 100% chance of their children developing NF). The severity in affected individuals can vary; this may be due to variable expressivity. Approximately half of cases are due to de novo mutations and no other affected family members are seen. It affects males and females equally. In addition, some individuals may have mosaic NF, in which some but not all cells of the body carry the mutation. The neurofibromatoses are as follows: ▪ Neurofibromatosis type I, in which the nerve tissue grows tumors (neurofibromas) that may be benign and may cause serious damage by compressing nerves and other tissues.

Definisi neurofibromatosis dalam kamus Corsica

Definisi neurofibromatosis dalam kamus adalah keadaan yang dicirikan oleh pembentukan tumor jinak pada penutup berserat saraf periferal dan pembangunan kawasan kafe-au-lait tempat.

TERJEMAHAN NEUROFIBROMATOSIS

Cari terjemahan neurofibromatosis kepada 25 bahasa dengan penterjemah Corsica pelbagai bahasa kami.

Terjemahan neurofibromatosis dari Corsica ke bahasa lain yang dibentangkan dalam bahagian ini telah diperolehi menerusi terjemahan statistik automatik; di mana unit terjemahan penting adalah perkataan «neurofibromatosis» dalam Corsica.

• Penterjemah Corsica - Cina: 神经纤维瘤病
• Penterjemah Corsica - Czech: neurofibromatosis
• Corsica: neurofibromatosis
• Penterjemah Corsica - Hindi: neurofibromatosis
• Penterjemah Corsica - Amhara: الورم العصبي الليفي
• Penterjemah Corsica - Rusia: нейрофиброматоз
• Penterjemah Corsica - Punjabi: neurofibromatose
• Penterjemah Corsica - Basque: neurofibromatosis
• Penterjemah Corsica - Frisia: neurofibromatose
• Penterjemah Corsica - Melayu: Neurofibromatosis
• Penterjemah Corsica - Chichewa: Neurofibromatose
• Penterjemah Corsica - Jepun: 神経線維腫症
• Penterjemah Corsica - Kreol Haiti: 신경 섬유종증
• Penterjemah Corsica - Jerman: Neurofibromatosis
• Penterjemah Corsica - Vietnam: neurofibromatosis
• Penterjemah Corsica - Tagalog: நியூரோஃபிப்ரோடோசிஸ்
• Penterjemah Corsica - Marathi: न्यूरोफिब्रोमेटोसिस
• Penterjemah Corsica - Turki: nörofibromatozis
• Penterjemah Corsica - Itali: neurofibromatosi
• Penterjemah Corsica - Poland: nerwiakowłókniakowatość
• Penterjemah Corsica - Ukraine: нейрофіброматоз
• Penterjemah Corsica - Romania: neurofibromatoza
• Penterjemah Corsica - Cina: νευροϊνωμάτωση
• Penterjemah Corsica - Afrikaans: neurofibromatose
• Penterjemah Corsica - Swahili: neurofibromatos
• Penterjemah Corsica - Parsi: Nevrofibromatose

CORSICA BUKU YANG BERKAIT DENGAN «NEUROFIBROMATOSIS»

Ketahui penggunaan neurofibromatosis dalam pilihan bibliografi berikut. Buku yang berkait dengan neurofibromatosis dan ekstrak ringkas dari yang sama untuk menyediakan konteks penggunaannya dalam kesusasteraan Corsica.

Neurofibromatosis: A Handbook for Patients, Families and ...

Here is the state-of-the-art on recognizing, managing and living with neurofibromatosis (NF) for patients, families, and health care professionals.

Bruce R. Korf, Allen E. Rubenstein, 2011

Neurofibromatosis: phenotype, natural history, and pathogenesis

" -- Journal of Medical Genetics "This is a comprehensive review of an extremely complex and pleomorphic disease.

Jan Marshall Friedman, Vincent M. Riccardi, 1999

Neurofibromatosis Type 1 in Childhood

A thoughtful and clinically valuable account which will aid both treatment of and research into this difficult disorder.

Kathryn North, 1997

Neurofibromatosis Type 1: New Insights for the Healthcare ...

Neurofibromatosis Type 1: New Insights for the Healthcare Professional: 2011 Edition is a ScholarlyPaper™ that delivers timely, authoritative, and intensively focused information about Neurofibromatosis Type 1 in a compact format.

‎2012

Neurofibromatosis: New Insights for the Healthcare ...

The editors have built Neurofibromatosis: New Insights for the Healthcare Professional: 2013 Edition on the vast information databases of ScholarlyNews.™ You can expect the information about Additional Research in this book to be deeper ...

‎2013

Biallelic Mismatch Repair Gene Mutations in a ...

Biallelic mismatch repair (MMR) gene mutations cause a distinct clinical syndrome that predisposes individuals to childhood-onset brain tumors, leukemia, lymphoma and gastrointestinal cancers.

Sarah Waltho, 2009

Neurofibromatosis Type 1: Molecular and Cellular Biology

Germline loss of function mutations in SPREDl cause a neurofibromatosis 1-like phenotype. Nat Genet 3911120—1126 Crawford AH Jr, Bagamery N (1988) Osseous manifestations of neurofibromatosis in childhood. J Pediatr Orthop ...

Meena Upadhyaya, David N Cooper, 2013

Rising Above: Facing the Dragon of Neurofibromatosis

Thus began my quest to find help for my daughter—one that would take many unexpected and nearly tragic turns.Rising Above: Facing the Dragon of Neurofibromatosisis the true account of Beth's indomitable, uplifting spirit while coping with ...

Janet Damon, 2012

Pathogenesis of Neurofibromatosis 1 Associated Neurofibromas

Neurofibromatosis 1 (NF1) is an autosomal dominant disease.

Tracy Tucker, 2007

Tumors of the Pediatric Central Nervous System

Highlights of the Second Edition: Contains 19 new chapters on such topics as recent advances in the cytogenetics and molecular biology of pediatric brain tumors, gangliogliomas and miscellaneous spinal cord tumors in children, post ...

Robert F Keating, James Tait Goodrich, 2013

BARANGAN BERITA YANG TERMASUK TERMA «NEUROFIBROMATOSIS»

Ketahui apa yang diterbitkan oleh akhbar nasional dan antarabangsa dan cara istilah neurofibromatosis digunakan dalam konteks perkara berita berikut.

Sydney mum starts social media campaign to find daughter's stolen …

Rachel Skelton and her 14-month-old baby Bella, who suffers from a genetic disorder called neurofibromatosis, were moving to Sydney to be ... «Daily Mail, Jul 15»

Adam Pearson reveals cruel treatment at hands of bullies in The …

Adam - who has neurofibromatosis type 1 which causes benign tumours to grow in the nerves on his face - was assaulted by the thug on a ... «Mirror.co.uk, Jul 15»

Mum's agony over her three boys living with genetic ticking time …

For Sam is a carrier of the genetic disorder neurofibromatosis type 1 (NF1), which can trigger the growth of brain tumours and lead to cancer ... «Mirror.co.uk, Jul 15»

Adam Pearson, who suffers from neurofibromatosis, wants to …

This is one of the few unmissable programmes of the week, written and presented by Adam Pearson. He suffers from neurofibromatosis and ... «The Times, Jul 15»

Thursday's TV tips

Actor Adam Pearson has Neurofibromatosis – a genetic condition that causes non-cancerous tumours to grow along his nerve endings. «Irish Examiner, Jul 15»

Active Stocks Traders Alert: Mack Cali Realty Corp (NYSE:CLI …

... investigated in a Phase 3 study in differentiated thyroid cancer and in a Phase 2 registration study in patients with neurofibromatosis Type 1. «wsnewspublishers, Jul 15»

​TV Tonight: The best things to watch on Thursday, July 23

Actor Adam Pearson has Neurofibromatosis – a genetic condition that causes non-cancerous tumours to grow along his nerve endings. «Western Morning News, Jul 15»

Selumetinib Misses Endpoint in Phase III Uveal Melanoma Study

Additionally, a phase II study is assessing the drug for patients with neurofibromatosis Type 1. "Selumetinib is supported by a strong ... «OncLive, Jul 15»

Finding may aid diagnosis of learning disabilities linked to brain …

More information: "Elucidating the impact of neurofibromatosis-1 germline mutations on neurofibromin function and dopamine-based learning. «Medical Xpress, Jul 15»

AstraZeneca Experimental Eye Cancer Drug Selumetinib Fails Late …

The drug is also being investigated as treatment for other malignant diseases such as thyroid cancer and neurofibromatosis, which is the ... «Tech Times, Jul 15»