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Most cases of Temporal Triangular Alopecia are found in early childhood and may be related to genetic conditions.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Loose Anagen Hair Syndrome is a hereditary condition causing hair loss in children due to abnormal hair follicles.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

Asian hair loss differs from Europeans; consider individual needs and psychological well-being for treatment.

The document explains hair growth and shedding, factors affecting it, and methods to evaluate hair loss, emphasizing the importance of skin biopsy for diagnosis.

Finasteride increases hair density in female androgenetic alopecia, but individual results may vary.

The document concludes that Nonclassic Congenital Adrenal Hyperplasia requires personalized treatment plans to manage symptoms and fertility, with glucocorticoids being a common therapy.

Finasteride might lower the risk of low-grade prostate cancer but not high-grade cancer, while alpha-blockers might reduce high-grade cancer risk.

The study suggests that motor neurons created from stem cells of patients with spinal and bulbar muscular atrophy show signs of the disease, including changes in protein levels and cell functions.

Cosmetics enhance beauty, fix defects, and intimidate enemies, with varying cultural standards and alternative methods.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Some plants used in traditional medicine may help treat cancer because they contain proteins that can inactivate ribosomes.

The document suggests using standardized methods to track and measure hair loss in alopecia areata, including patient self-assessment and a 50% improvement in specific scores as a treatment goal.

Patient had scalp allergy from minoxidil; test helped identify cause and suggest alternative treatments.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Sweat glands and hair follicles are structurally connected within a specific layer of skin fat.

A male with aromatase deficiency improved bone health with estradiol treatment.

The document suggests that the traditional understanding of hair growth cycles and alopecia may be inaccurate and that blood supply plays a significant role in hair growth and loss.

DHT's role in hair loss is important, but measuring its level for diagnosis is questionable.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Longer hair loss leads to more severe CCCA; early treatment and avoiding damaging hairstyles help regrowth.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

At least 87% of Indian men experience hair loss, with type II being most common and severity increasing with age.

Infertile men are more likely to produce sperm with abnormal chromosome numbers, which can affect pregnancy success and embryo health.

Using neurohormones to control keratin can lead to new skin disease treatments.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

Acitretin is effective for severe psoriasis and can be used long-term due to no immunosuppression, but must be carefully monitored for side effects and is not for pregnant women.

Early diagnosis and aggressive treatment are crucial for better outcomes in lymphomatoid granulomatosis.