Search | Humwaten pakistan Ist social website

Vaishnavi Cmi added article Health
2024-06-13 06:41:45

Advances in Duchenne Muscular Dystrophy Treatment
Causes and Mechanism of Duchenne Muscular Dystrophy Duchenne muscular dystrophy (DMD) is a genetic disorder characterized by progressive muscle degeneration and weakness. It is caused by the absence of dystrophin, a protein that helps keep muscle cells intact. The defective gene that causes DMD is located on the X chromosome, so it primarily affects boys. Girls can be carriers of the defective...

0 Comments 0 Shares 281 Views

Please log in to like, share and comment!
Raj Dhote added article Other
2024-04-12 12:30:13

Exploring The Global Landscape Of Antisense & Rnai Therapeutics
Antisense and RNAi therapeutics are at the forefront of medical innovation, offering a new approach to treating genetic disorders, cancers, and other diseases. These therapies have gained significant attention worldwide due to their precision and potential impact on healthcare. In this article, we'll explore the global landscape of antisense and RNAi therapeutics, including trends, key players,...

0 Comments 0 Shares 502 Views

Please log in to like, share and comment!
Raj Dhote added article Other
2024-04-26 11:53:24

Exploring The Potential Global Antisense & Rnai Therapeutics In Medicine
In recent years, the fields of antisense therapeutics and RNA interference (RNAi) have emerged as promising approaches for treating a wide range of diseases, including genetic disorders, viral infections, and certain types of cancer. These innovative technologies harness the power of nucleic acids to modulate gene expression, offering new avenues for targeted therapy and personalized medicine....

0 Comments 0 Shares 408 Views

Please log in to like, share and comment!
CMI Blogging added article Health
2024-04-29 11:05:29

Global Leigh Syndrome Treatment Market is Estimated to Witness High Growth Owing to Advancement in Gene Therapy
The global Leigh syndrome treatment market is witnessing high growth owing to the advancement in gene therapy. Leigh syndrome is a rare neurological genetic disorder that affects the central nervous system and metabolism. It is usually seen in infants and children under the age of 2. The signs and symptoms associated with Leigh syndrome include poor muscle tone, muscle weakness, vision issues,...

0 Comments 0 Shares 509 Views

Please log in to like, share and comment!
Sneha Biswal added article Other
2024-04-23 13:54:17

Hereditary Orotic Aciduria: An Overview of a Rare Genetic Disorder
Hereditary orotic aciduria is a rare inherited genetic disorder that affects pyrimidine nucleotide synthesis in the body. It is caused by a mutation in the UMPS gene that encodes for the enzyme orotate phosphoribosyltransferase (OPRT). This enzyme plays a vital role in the pyrimidine salvage pathway involved in the biosynthesis of uridine monophosphate (UMP), which is required for the formation...

0 Comments 0 Shares 427 Views

Please log in to like, share and comment!
Sneha Biswal added article Other
2024-04-26 12:29:05

Morquio Syndrome (MPS-IV) Drug: Updates on Treatment Options for Rare Genetic Disorder Morquio Syndrome
Morquio syndrome, also known as mucopolysaccharidosis type IV (MPS-IV), is a rare inherited lysosomal storage disease caused by deficiency of the enzyme N-acetylgalactosamine 6-sulfatase (GALNS). This enzyme is responsible for breaking down glycosaminoglycans (GAGs), long chains of sugar molecules important for healthy cellular functioning. Without sufficient GALNS enzyme activity, GAGs...

0 Comments 0 Shares 554 Views

Please log in to like, share and comment!
Raj Dhote added article Other
2024-04-22 10:48:14

Navigating Life with Global Spastic Paraplegia 50: Coping Strategies and Support Resources
Global Spastic Paraplegia 50 (GSP50) can present unique challenges for individuals and families, but with the right support and resources, it's possible to navigate life with this rare genetic disorder. This article explores coping strategies and available support resources for those affected by GSP50. Coping Strategies: Coping with the daily challenges of Global Spastic Paraplegia 50 requires...

0 Comments 0 Shares 445 Views

Please log in to like, share and comment!
Raj Dhote added article Other
2024-05-17 12:55:22

Navigating U.S. Receiving A Diagnosis Of Urea Cycle Disorders: A Comprehensive Guide
Receiving a diagnosis of Urea Cycle Disorders (UCDs) can be overwhelming, but understanding the treatment options and available resources is essential for effectively managing these rare genetic conditions. Let's explore a comprehensive guide to navigating UCDs treatment in the United States, along with sub-points for each aspect: Specialized Medical Care Finding Specialists: Seek out...

0 Comments 0 Shares 387 Views

Please log in to like, share and comment!
Raj Dhote added article Other
2024-04-15 10:57:17

Perspectives On Global Spastic Paraplegia 50: Challenges And Opportunities
Spastic paraplegia 50 (SPG50) is a rare, inherited neurological disorder that causes progressive weakness and spasticity in the lower limbs. It's caused by mutations in the AP4M1 gene and is a subtype of hereditary spastic paraplegia (HSP). In this article, we explore the Spastic paraplegia 50 (SPG50) is a rare genetic disorder that affects the nervous system, causing progressive weakness and...

0 Comments 0 Shares 381 Views

Please log in to like, share and comment!
Raj Dhote added article Other
2024-04-23 11:53:11

The Rising Influence Of Global Antisense And Rnai Therapeutics In Precision Medicine
Antisense therapeutics and RNA interference (RNAi) have emerged as transformative approaches in precision medicine, offering targeted therapies for a wide range of diseases by modulating gene expression at the molecular level. These innovative technologies hold promise for treating genetic disorders, viral infections, neurodegenerative diseases, and cancer, among other conditions. Let's explore...

0 Comments 0 Shares 364 Views

Please log in to like, share and comment!

More Results