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Fibrinogen/LDL apheresis may improve speech perception in sudden hearing loss, especially for those with high fibrinogen and LDL levels.

Activating Nrf2 can help protect against hearing loss.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

The document explains the genetic causes and characteristics of inherited hair disorders.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Patients with Bohring-Opitz syndrome and ASXL1 mutations need regular kidney ultrasounds to check for tumors.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

Long-COVID has diverse, long-term health impacts, especially in young people.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

People with Down syndrome have higher rates of certain immune-related conditions and need special medical attention.

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

The document is a detailed medical reference on skin and genetic disorders.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Asia has made significant progress in tissue engineering and regenerative medicine, but wider clinical use requires more development.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

Piezoelectric Nanogenerators are promising for non-invasive health monitoring but need efficiency and durability improvements.

The conclusion is that genetic differences affect how the cochlea heals after hair cell loss, which may challenge the creation of hearing loss treatments.

Advanced hydrogel systems with therapeutic agents could greatly improve acute and chronic wound treatment.

A model called PM-DBiGRU was developed for analyzing sentiments in drug reviews, and it performed better than other models, but struggled with complex sentences and situations requiring background knowledge.

Choline and biotin are important for liver health and preventing certain deficiencies in animals, and more research is needed to understand their benefits in humans.

Conductive hydrogels show promise for medical uses like healing wounds and tissue regeneration but need improvements in safety and stability.

Hydrogels combined with extracellular vesicles and 3D bioprinting improve wound healing.

Special gels help heal diabetic foot sores and reduce the risk of amputation or death.