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The study suggests that a new protease inhibitor can make hair harder to pull out, potentially reducing hair loss.

The European Society of Endocrinology advises individualized long-term management for PCOS, focusing on lifestyle changes, accurate diagnosis, and treatments for associated health risks and symptoms.

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

Genetic factors could lead to personalized treatments for hair loss.

Hair growth serums A and C can affect hair growth genes and pathways, suggesting potential for personalized hair loss treatments.

Different genes cause Female Pattern Hair Loss compared to male hair loss, and treatments vary, but more research is needed to understand it fully.

Minoxidil, finasteride, and low-level laser light therapy are effective FDA-approved treatments for hair loss.

The conclusion is that formalizing how past decisions influence current health technology assessments could improve the credibility and defense of coverage decisions.

Personalized treatments for hair loss are becoming more effective by using genetic information.

The document concludes that MGRN1 affects mouse fur color by interfering with a receptor's signaling, but its full role in the body is still unknown.

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

Gene mutations can cause problems in male genital development.

Women with type 1 diabetes often have polycystic ovary syndrome and excess male hormones, which are frequently undiagnosed.

Sex hormones affect hair growth and loss, and treatments for related hair diseases include various medications, hair transplantation, and light therapy.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Keratin mutations cause skin diseases and could lead to new treatments.

Blocking certain immune signals can reduce skin damage from radiation therapy.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

Multiple treatments work best for hair loss.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

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.

Scalp basal cell carcinoma may be more aggressive and harder to treat than other types, requiring special attention and further research.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

More research is needed to understand the genetic causes of Alopecia areata to develop better treatments.

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

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.

Genetic factors affect hair loss, and molecular testing may help predict, diagnose, and treat it.