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Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

Leptin helps start the growth phase of hair.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Scientists made skin stem cells from other human cells with over 97% efficiency, which could help treat skin conditions.

The document concludes that unruly hair can be congenital or acquired, often lacks specific treatments, and can be managed with oils and short hairstyles.

Children with short anagen syndrome usually see their hair condition improve as they get older.

Alopecia areata causes varying hair loss patterns, affecting hair, nails, and possibly glands, with treatment outcomes depending on disease duration and extent.

PGA-4HGF may help treat hair loss by activating hair growth pathways and extending the hair growth phase.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

A young cat had a rare hair condition with twisted hair shafts but stayed healthy.

Taking vitamins, minerals, and amino acids can improve hair strength and quality in people with Monilethrix.

NF-κB signaling is crucial in many diseases and can be targeted for new treatments.

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

Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

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

Stopping forehead irritation and using hydrocortisone helped a man's skin, Martinique has lower melanoma rates, a man had an allergy to a specific antifungal, another had unexplained cysts, certain drugs can cause skin reactions without always being interrelated, a link between Fanconi anemia and a skin condition was suggested, high levels of a certain protein may play a role in a type of psoriasis, and there's a need to study the connection between scalp pain and hair loss.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

Platelet-rich plasma (PRP) is a simple, cost-effective treatment that promotes hair growth and reduces hair loss, with high patient satisfaction.

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

Most hospitalized children with skin issues were boys, with allergic skin diseases like atopic dermatitis being most common, and treatments were usually topical.

Sox2 controls hair color by affecting pigment production in hair follicles.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

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

BMP signaling controls hair follicle size and cell growth by affecting cell cycle genes.

Edar signaling is crucial for proper hair follicle development and function.

Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.