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Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

The study concluded that genetic mutations affect human hair diseases and identified key genes and pathways involved in hair growth and cycling.

Two siblings have a rare genetic condition causing curly, coarse hair.

Hair loss in women is genetic, diagnosed by examination and biopsy, and treated with minoxidil, finasteride, or transplantation.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

A genetic marker linked to a type of hair loss was found in most patients studied.

The document explains the genetic causes and characteristics of inherited hair disorders.

Botanical extracts can help treat hair loss in people with certain genetic conditions.

Certain genetic variants in PRLR and PCCA genes may lead to shorter hair in cattle, which could help with heat tolerance.

Certain genetic variations are linked to hair loss in Mexican men.

Avoiding smoking, stress, obesity, and poor diet may help reduce hair loss in young Egyptian males.

Scientists found new genetic areas that affect how rice root hairs grow and develop.

Minoxidil improved hair growth in a child with a rare genetic disorder.

Hair color is determined by melanin and can be affected by genetic conditions like albinism.

Androgenetic alopecia is mainly caused by genetic factors and increased androgen activity, leading to hair follicle miniaturization.

Women with greater androgen sensitivity respond better to finasteride for hair loss.

Low-dose radiation affects hair stem cell function and survival by changing their genetic material's structure.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

External factors like certain shampoos, bacterial infections, and parasites might cause hair defects similar to genetic conditions.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

The research found that a protein called PPARg is important for the formation and healing of sebaceous glands, which can regenerate independently from hair follicles.

A 21-year-old male with a rare genetic disorder experienced sudden hair loss and high DHEAS levels, likely due to a condition similar to PCOS, usually seen in women.

Hair loss in women often doesn't follow a pattern, isn't linked to age, may be genetic, and can be related to thyroid issues or other health factors.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

The document concludes that new treatments for hair loss may involve a combination of cosmetics, clinical methods, and genetic approaches.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

The conclusion is that hair loss in women is caused by a mix of hormonal, environmental, and genetic factors, and treatments should target these various causes.

Hair loss without scarring is more common than permanent hair loss with scarring, and is often due to genetic factors.

Researchers found new hair and nail genes, how hair reacts to UV, differences in white and pigmented hair growth, nerve changes in alopecia, treatments for baldness and alopecia, a toenail condition linked to a genetic disorder, and that nail fungus is more common in people with psoriasis.