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

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

Epigenetic factors play a crucial role in skin health and disease.

The document concludes that using stem cells to regenerate hair follicles could be a promising treatment for hair loss, but there are still challenges to overcome before it can be used clinically.

FGF13 gene changes cause excessive hair growth in a rare condition.

The main causes of diffuse hair loss in women are telogen effluvium and androgenetic alopecia, often related to stress and iron deficiency.

Intralesional triamcinolone injections can effectively stop frontal fibrosing alopecia with minimal side effects.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Scientists made structures that look like human hair follicles using stem cells, which could help grow hair without using actual human tissue.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Stem cells and their exosomes show promise for repairing tissues and healing wounds when delivered effectively, but more research is needed on their tracking and optimal use.

Hair microscopy is a simple and cost-effective method to help diagnose systemic diseases in children.

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

DFMO treatment improves hair growth, muscle tone, and development in Bachmann-Bupp syndrome patients.

PRP therapy for hair loss is safe but its effectiveness is doubtful.

PRP generally shows better results for hair regrowth than mesotherapy, but more research is needed.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Hair follicles are normally protected from the immune system, but when this protection fails, it can cause hair loss in alopecia areata.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

The project created a standardized system for classifying skin lesions in lab rats and mice.

Disrupting β-catenin signaling in certain cells causes anorectal malformations.

Odontogenic keratocysts are caused by abnormal Hedgehog signaling and can lead to tooth and bone issues.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

Skin organoids from stem cells could better mimic real skin but face challenges.

Minoxidil may help treat hair loss by reducing inflammation-related gene activity in skin cells.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Growth factors greatly affect hair loss, with different levels seen in men, women, younger patients, and at the start of the condition.