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Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

Hair disorders are caused by a complex mix of biology, genetics, hormones, and environmental factors, affecting hair growth and leading to conditions like alopecia.

Hair loss involves immune responses, inflammation, and disrupted signaling pathways.

Vitamin D receptor helps control hair growth genes in skin cells.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Histone demethylases play a key role in the development of many diseases and may be targets for treatment.

A spermidine-based supplement may help hair grow longer by keeping it in the growth phase.

The review concludes that accurate diagnosis of different types of hair loss requires proper biopsy techniques and understanding the hair growth cycle and underlying causes.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

The commentary explains that a balance of HR protein and putrescine is important for normal hair growth.

The document concludes that proper diagnosis and management of hair loss in children require a detailed examination and understanding of various hair disorders.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

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.

The document concludes that understanding hair biology and recognizing hair conditions are crucial for managing and treating hair loss in children.

Minoxidil treats hair loss, promotes growth, has side effects, and has recent patents.

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

The Hairless gene is crucial for hair cell development, affecting whether skin cells become hair or skin and oil gland cells.

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.

FFA's causes may include environmental triggers and genetic factors.

Hair ages and thins due to factors like inflammation and stress, and treatments like antioxidants and hormones might improve hair health.

Mice with a changed Hr gene lose and regrow hair due to changes in the gene's activity.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

The document describes the signs of different common types of hair loss.

Hairless protein reduces Msx2 gene activity, affecting hair follicle development.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.