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

Mice without certain skin proteins had abnormal skin and hair development.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

Some breast cancer patients developed permanent hair loss after chemotherapy and hormonal therapy, showing patterns similar to common baldness and alopecia areata.

The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

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.

Teriflunomide is effective and generally safe for treating relapsing-remitting multiple sclerosis.

Cyclosporine A promotes hair growth and prolongs the active growth phase in human hair follicles, but may work differently than in rodents.

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

Doctors have known about fungal skin infections for a long time, but only made major progress in understanding and treating them since the mid-1800s.

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

The document concludes that using specific tools and tests is essential for identifying the cause of hair loss and deciding on the right treatment.

Diphencyprone treatment increases CD8 lymphocytes in the scalp, which is associated with hair regrowth in alopecia areata patients.

ICL is a condition with low CD4+ T cells like AIDS but not caused by HIV, and normal CD4+ T cell counts may vary between men and women.

The document concludes that supportive home environments and addressing parent-child interactions can effectively treat trichotillomania in children.

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

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.

Hedgehog signaling is crucial for mammary gland development over hair follicles.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

The environment around melanocyte stem cells is key for hair regeneration and color, with certain injuries affecting hair color and potential treatments for pigmentation disorders.

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

Gene linked to common hair loss found, may lead to new treatments.

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

ARL15 is important for fat cell development and the release of the hormone adiponectin.

Coating surfaces with human hair keratin improves the growth and consistency of important stem cells for medical use.

Minoxidil 2% effectively treats Monilethrix without side effects.