Search

everythinglearnresearchcommunity

for

Search:↓

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

Different fields of expertise must work together to better understand hair growth and create effective hair loss treatments.

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

VEGF helps squamous cell carcinoma grow in ways beyond just blood vessel formation.

Monilethrix causes different levels of hair loss in family members.

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

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.

The most common causes of hair loss in Jordanian children are fungal infections, autoimmune hair loss, and hair shedding after fever, with zinc deficiency also being a notable cause.

A 5-year-old girl has sparse, dry, and brittle hair but is otherwise healthy.

Hair loss can indicate underlying systemic diseases and addressing these can sometimes reverse the hair loss.

Hair care products are important for appearance and self-esteem, and choosing the right ones can help maintain healthy hair.

Rectangular black granules, solitary yellow dots, and mostly single-hair follicles suggest Loose Anagen Hair Syndrome.

Hair follicles are important for drug delivery through the skin, but better methods are needed to understand and improve this process.

The document concludes that skin stem cells are important for hair growth and wound healing, and could be used in regenerative medicine.

The conclusion is that the best approach for treating Female Pattern Hair Loss is a combination of different treatments.

Lipase H is important for hair follicle function and shaping hair fibers.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

About 12% of children in Kota, Rajasthan, experience hair loss, mainly due to fungal infections, with early treatment advised to prevent worsening.

Transfollicular drug delivery is promising but needs more research to improve and understand it better.

Trichoscopy, a hair loss evaluation technique, found that people with Androgenetic Alopecia have more thin hairs, yellow dots, and perifollicular discoloration than healthy individuals.

Androgenetic alopecia causes hair thinning due to increased androgen activity, treatable with minoxidil and finasteride.

Trichoscopy is good for telling apart tinea capitis and alopecia areata in kids.

Recent discoveries have improved our understanding of hair loss, but challenges in treatment and knowledge among specialists still exist.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

Hair thinning and loss in a girl with a rare metabolic disorder was linked to her condition.

A woman's hair changed to a dry, tangled texture that's hard to comb after treatment with spironolactone, suggesting the medication might cause such hair changes.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

The Hairless gene is crucial for healthy skin and hair growth.