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Biotinidase deficiency has various symptoms and can be treated with biotin supplements.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Heavy metals might contribute to hair loss in Telogen Effluvium.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Different stem cells are key for hair growth and health, and understanding their regulation could help treat hair loss.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

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

Balanced hormones are crucial for women's health, and can be managed with lifestyle changes or hormone therapy if needed.

Macrophage activation syndrome can be a deadly first sign of systemic lupus erythematosus.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

Isotretinoin therapy for acne can cause many reversible side effects, mainly mild skin conditions, and patient understanding of these effects can improve treatment adherence.

Autologous Platelet and Extracellular Vesicle-Rich Plasma (PVRP) has potential in enhancing tissue regeneration and improving hair conditions, but its effectiveness varies due to individual differences.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Satoyoshi syndrome can cause eye problems like uveitis and retinal vein issues.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

Regenerative cosmetics can improve skin and hair by reducing wrinkles, healing wounds, and promoting hair growth.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

The study concludes that regulating apoptosis could lead to new treatments for various skin and hair conditions.

Gene therapy, especially using atoh1, shows promise for creating functional sensory hair cells in the inner ear, but dosing and side effects need to be managed for clinical application.

Blond hair in Solomon Islanders is due to a unique genetic variant, not European ancestry.

Hair grays due to oxidative stress and fewer functioning melanocytes.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

Children are at risk of health issues from exposure to platinum group elements from car exhausts.

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

Epipharyngeal Abrasive Therapy helps reduce symptoms in Long COVID patients with chronic epipharyngitis.

In Denmark from 1995 to 2016, hospital-treated alopecia areata cases increased, mostly affecting women and those over 50.