6th International Conference on Rare Diseases and Orphan Drug

-



 


We are so glad to organize “6th International Conference on Rare Diseases and Orphan Drug” in Dubai,UAE on February 18-19, 2019 with the theme “Challenges and opportunities in elimination of Rare diseases & orphan development”.


This two days of Rare Diseases Meet 2019 will offer an interactive and most compressive session & networking with global experts working in the Rare Disease & Orphan Drugs segment. Rare Diseases Meet 2019 Dubai Conference will help in gaining insights & to upgrade knowledge towards current activities growing globally in the Orphan Drugs sector starting from Laboratory research to field research, clinical trials to orphan drugs development, pricing and reimbursement, commercialization of orphan drugs & regulatory policies etc. Rare Diseases Meet 2019 comprises of well-organized scientific program stuffed with interactive sessions, one to one discussion rounds, industry-academia interaction programs, industrial presentations, special regulatory sessions, and networking sessions.

Rare Diseases Meet 2019 provides a technical forum for learning about the latest and advanced research and development. This contains finest topics like Rare Diseases and orphan drug presentations from all over the world with industries, and panel.


Most Targetable audience in our conference are Neurologists,  Anesthesiologists, Cardiologists, Ophthalmologists, Healthcare professionals, Epidemiologists, Microbiologists, Pathologists, Bacteriologists, Virologists, Parasitologists, Pharmacists, Medical colleges, Medical Devices Manufacturing Companies, Drug Manufacturing Companies and Industries, Laboratory Technicians and Diagnostic Companies, Business Entrepreneurs and Industrialists, Rare disease Association & Societies, Scientists who explore their research work.

In Rare Diseases Meet 2019 organize with various hot topic which are highlighted our conference. These are Mystery Diagnosis of Rare Diseases, Rare Brain Disorders, Rare Oncology Diseases, Rare Genetic Diseases, Rare Skin Diseases, Rare Diseases in Anesthesiology, Rare Pulmonary Diseases, Rare Obstetrical Diseases, Rare Oral Diseases, Rare Hematological Diseases, Rare Aging Diseases, Rare Metabolic Diseases, Rare Diseases of Genitourinary System, Rare Musculoskeletal Diseases, Rare Pediatric Diseases, Rare Diseases of Endocrine System, Rare Cardiac Diseases, Orphan Drugs- Development Trends and Strategies, Drug Approvals for Rare Diseases, Future Hereditary of Rare Diseases and Orphan Drugs.

Comments

Post a Comment

Popular posts from this blog

Read This Controversial blog And Find Out More About TAY-SACHS DISEASE

-
Image
Tay-Sachs disease is a rare, inherited disease . It is a type of lipid metabolism disorder in which deficiency of an enzyme ( hexosaminidase A ) results in excessive accumulation of certain fats (lipids) known as gangliosides in the brain and nerve cells. It makes a lot of a fatty substance to develop in the brain. This development ruins nerve cells, causing mental and physical complications. Maximum people have two healthy sorts of this HEXA gene, which provides guidelines to your body to make an enzyme (a type of protein) known as Hex-A. This enzyme inhibits the development of a fatty substance, called GM2 ganglioside, in the brain and spinal cord. Infants usually begin to show signs of the disease between 3 months and 6 months of age. Children with Tay-Sachs disease can become deaf, blind and paralyzed, and generally die by the age of 5. Tay-sachs is named after two physicians Warren Tay, was an ophthalmologist who was the first to determine a red dot on the retina of on...
Read more

Rare Diseases of Endocrine System

-
Image
Gigantism Gigantism also called gigantism obtained from a Greek word gigas, is a Rare Endocrine Diseases characterized by excessive growth hormone which accelerates the growth of muscle, bones and connective tissue in childhood or youth before the end of puberty. It is always the consequence of a growth hormone secreting pituitary tumour. When left untreated or uncontrolled, some individuals suffering from gigantism have grown in excess of eight feet (2.4 m) tall. The most well-known example is that of Robert Wadlow, the tallest person in history. Cause Most common reason of gigantism is Pituitary gland tumor . The pea sized pituitary gland is located at the base of the brain; it makes hormones that control body temperature, metabolism growth, sexual development and urine production. Some other cause of gigantism is: ·          McCune-Albright disease is a disorder that causes unusual growth of bone tissues, gland irregu...
Read more

Sesquizygotic Twinning: What No One Is Talking About

-
Image
Multiple births are progressively basic due to the advancing normal time of mothers and the related ascent in helped regenerative techniques, specifically the utilization of fertility drugs . Twins represent over 90% of numerous births. Twins are usually categorized into two that is – identical ( monozygotic ) and fraternal ( dizygotic ). Monozygotic twinning results in genetically identical individuals, whereas dizygotic twins share approximately 50% of their DNA sequence identity, as do full siblings. Sesquizygosity is a third form of rare twinning — whereby twins are genetically identical to each other with respect to one parent but differ from each other by approximately 50% with respect to the composition of DNA inherited from the other parent. It probably arises after heterogoneic assortment of two paternal genomes and one maternal genome during the first postzygotic cleavage division. Genetically, sesquizygosis can be viewed as on a continuum among monozygosis and...
Read more