Call for Abstract


December 04-05, 2023 | 08:00 AM SGT


Dubai, UAE

Speakers Interview

Scientfic Sessions:

Any illness that affects a very small percentage of the population is considered rare. Rare diseases include uncommon cancers, such as childhood cancers, as well as certain other well-known disorders, such as cystic fibrosisCF, pancreatic fibrosis, mucoviscididosis, fibrosis, and monogenic disorder. Huntington's disease and monogenic disease.
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Unusually, several words are used to describe infectious diseases. An infectious disease is an ailment brought on by an organism, and illness is the presence of pathology. The ability of an organism to cause illness in a given host is referred to as virulence. The level of the host's resistance to a specific germ is referred to as immunity. Vaccines prevent various infectious diseases, including varicella and morbilli.
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Rare cancers affect an incredibly small population of people. If a cancer begins in a unique location within the body, it may also be regarded as rare. Or if the cancer is a rare type that requires specialised care and is brought on by ad hoc changes in the body. Experts are unsure of what causes the mutation. Since many people may not exhibit symptoms until later stages, regular blood tests are all that is needed to make the identification.
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As eighty percent of rare diseases are caused by a single sequence and gene medical treatment has the potential to repair several genetic abnormalities, it is one of the reasonable strategies to treat rare sequencetic disorders. Restore one sequence defect by introducing a "right" sequence. Additionally, womb-to-tomb improvement may require only a single dosage of outstanding sequence medical therapy.
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Rare paediatric illnesses, which can be serious or fatal, affect people from birth to age 18, including the age groups often known as neonates, babies, children, and adolescents. One example of a paediatric rare disease is achondrogenesis Rare Diseases and Health.
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The majority of disorders that affect the skin start deep beneath its layers, and these anomalies are crucial in identifying a variety of internal diseases. The inherent region-specific anatomical variability of the skin can significantly alter how a rash appears. This becomes clear after skin is transplanted from one area of the body to another and still displays the morphological traits of the donor area. Hereditary skin illnesses are commonly categorised using gross morphological, histologic, and microscopic results; however, the precise diagnosis is frequently uncertain since skin diseases may not always appear in a recognisable way.
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The main link between brain illnesses and altered brain function or structure is this. this may be primarily due to seizures, state-of-mind, temperament changes, tumours, and infections. Jakob-Creutzfeldt disease (CJD) is an uncommon chronic brain disorder that is characterised by rapidly advancing medical conditions and severe symptoms. Once symptoms start, those who are impacted may experience disorientation, depression, changes in activity, reduced vision, and/or impaired coordination.
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Rare genetic diseases ar caused by one or a lot of abnormalities within the ordination. it should be caused thanks to mutation in a very single sequence or multiple genes. However, there aren't any proverbial treatments for genetic disorders. several genetic disorders influence stages of development like Down's syndrome, whereas others end in physical symptoms like hereditary condition. thanks to the wide selection of genetic disorders, identification is wide varied and looking on the disorder.
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RBC beta monogenic disorder, Diamond-Blackfan anaemia, and other anemia-type red vegetative cell conditions, white vegetative cell dysfunctions associated with various malignancies, and immuno-protoplasm-based abnormalities that affect platelet and lymphocyte disorders are just a few examples of the diverse subcategories of rare medical specialty diseases. Some rare blood illnesses, particularly those that are gene-based, can be distinguished with ease with a simple test, whilst others require substantial research to be properly analysed
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Due to the rarity and variety of rare infections, research must be conducted globally to ensure that experts, researchers, and doctors are connected and that clinical trials are conducted internationally so that patients can benefit from the pooling of resources across borders. Patients with rare illnesses still have to endure lengthy wait times in the healthcare system before a firm diagnosis is made.
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In later years, national and international associations are established to inform and protect patients affected by these ailments. Rare infections caused by systemic changes represent a field of life science that is very interesting and is constantly expanding. These disorders have a ludicrous social and economic impact because they typically affect young or severely ill children who are at the height of their social activities and relationships.
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Orphan drugs are a group. The medical product designated to treat rare diseases or unusual disorders and intended for the treatment, obstructing, or designation of a rare sickness or condition are called as "orphan medications" due to their niche markets. According to the definition of an orphan disease, it only affects 200,000 people nationwide. The majority of orphan diseases have a genetic basis. One in fifteen people could be affected by an orphan disease worldwide.
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There are numerous rare disorders of the body. According to the National Organization of Eudaimonia, over 175 different rare diseases affect the system, a complex system of organs and glands that uses about 30 different hormones to affect a variety of vital functions, including growth, metabolism, heart function, and fertility. Addison's disease is extremely rare. However, any organ system may likely be affected by rare endocrine illnesses.
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