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

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

Cancer development is like natural selection, involving mutated cells and environmental factors.

Skin grafts are effective for chronic leg ulcers, especially autologous split-thickness grafts for venous ulcers, but more data is needed for diabetic ulcers.

Keratins are important for skin cell health and their problems can cause diseases.

New methods to improve the healing abilities of mesenchymal stem cells for disease treatment are promising but need more research.

The document explains different types of hair loss, their causes, and treatments, and suggests future research areas.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.

Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

Female pattern hair loss has unclear causes, possibly involving genetics, hormones, and environment, and needs better treatments.

The gene KAP22-1 affects wool yield and fiber shape in sheep.

Female pattern hair loss involves hormonal factors, genetics, and may be linked to low ferritin levels.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

The document concludes that lifestyle changes and medical treatments can significantly reduce symptoms of Hidradenitis Suppurativa, a chronic skin condition.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

Skin aging is caused by stem cell damage and can potentially be delayed with treatments like antioxidants and stem cell therapy.

PCOS may start before birth, involves metabolic issues, and can be treated with drugs like metformin and lifestyle changes.

The study found that Central Centrifugal Cicatricial Alopecia mainly affects middle-aged African descent women, is linked to certain hair care practices and genetics, and often goes undiagnosed for years.

Methotrexate effectively treated a 2-year-old's generalized pustular psoriasis without side effects.

Thiopurines help treat IBD but require genetic testing to avoid side effects.

People with Inflammatory Bowel Disease often lose hair due to stress, medication side effects, or lack of nutrients, and treatment depends on the specific cause.

In vivo lineage labelling is better than in vitro methods for identifying and understanding stem cells.

New treatments and early diagnosis methods for permanent hair loss due to scar tissue are important for managing its psychological effects.

Gene regulation could revolutionize hair color by altering pigmentation from within.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

Alopecia areata causes hair loss due to an immune attack on hair follicles, influenced by genetics and environment.