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A 3-year-old boy lost all his hair due to a rare reaction to phenobarbital, but it grew back after steroid treatment.

Testosterone is crucial for development, growth, and various body functions in mammals.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Deleting the PTEN gene in mice causes nerve cells to grow larger and heal better after injury, but may cause overgrowth and hair loss in older mice.

Indian Gooseberry has potential for cancer prevention and treatment and promotes hair growth.

Blocking DGAT1 reduces oil gland size in mice and dogs, but only mice experience hair loss.

The proteins transthyretin and megalin are more present in the growth phase of hair, suggesting they might affect hair health and growth.

Rapamycin may help treat Leigh syndrome by targeting protein kinase C.

Hormonal therapies are safe and effective for treating acne in female adolescents, with specific treatments for those with endocrine disorders.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

Acne is a common skin condition that can be influenced by diet, lifestyle, and hormones, and requires a treatment approach that includes psychological considerations.

The skin protects the body, regulates temperature, senses touch, and makes vitamin D.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

The document describes various skin conditions, their features, and treatments but lacks detailed study size information.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

Genes related to keratin, skin cell differentiation, and immune functions are key in hedgehog skin and spine development.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

The conclusion is that different blood diseases cause specific oral symptoms and require varied treatments to manage these symptoms and improve patient health.

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.

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

Early treatment of acne is crucial to prevent scarring and psychological effects.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.

The document does not determine if adults with aphallia are fertile.

FLCN helps control iron levels in cells.

Hidradenitis Suppurativa is a chronic skin condition best treated early with surgery for better outcomes and less recurrence.