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Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

FGF13 gene changes cause excessive hair growth in a rare condition.

Five new mutations in the androgen receptor gene were found, helping to understand androgen insensitivity syndrome better.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Measuring reproductive hormones in brown bear hair could help identify their sex and reproductive state, but better collection methods or lab techniques are needed.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

ILK and ELMO2 help cells move and stick together, important for wound healing and hair growth.

Dutasteride is linked to a higher chance of sexual dysfunction, especially in younger males and the elderly.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

Using both hyaluronic acid compounds together improves skin hydration and reduces wrinkles better than using one alone.

The document concludes that hair keratin-chitosan scaffolds were successfully made and are suitable for biomedical use.

A hair-straightening product caused widespread hair loss and scalp injuries, mainly affecting African American women.

Certain skin conditions in women are linked to higher risks of metabolic syndrome and type 2 diabetes due to hormone imbalances.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

Hair loss in adults is linked to heart disease risk factors like unhealthy blood fats, lack of exercise, and alcohol use. It's also slightly more common in people with metabolic syndrome. As people age, hair loss gets worse. In men, severe hair loss is tied to high blood pressure and a larger waist. In women, it's tied to higher body weight. People with hair loss should be checked for unhealthy blood fats and advised to avoid alcohol and inactivity.

The study found unique skin changes in a rare type of alopecia linked to a skin condition called linear morphea.

The cancer drugs bortezomib and lenalidomide cause skin side effects in many patients.

Quetiapine may cause hair loss.

Alopecia areata is a genetic and immune-related hair loss condition that is often associated with other autoimmune diseases and does not typically cause permanent damage to hair follicles.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

Changes in keratin make hair follicles stiffer.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

The document concludes that more research is needed to better understand and treat primary cicatricial alopecias, and suggests a possible reclassification based on molecular pathways.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

Skin fat has important roles in hair growth, skin repair, immune defense, and aging, and could be targeted for skin and hair treatments.

New genetic discoveries may lead to better treatments for alopecia areata.

Blocking SCD1 in the skin with XEN103 shrinks sebaceous glands in mice.

Genetic discoveries are leading to new treatments for alopecia areata.