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Various treatments, including FDA-approved drugs, natural products, and oral supplements, can help with hair loss, but a patient's medical history and potential allergies should be considered when choosing a treatment.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

The document concludes that detailed clinical descriptions of seven family cases help understand dominant dystrophic epidermolysis bullosa's symptoms and inheritance.

The topical inhibitor CUR61414 was not effective in treating basal cell carcinoma in human trials.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

An apple-based supplement was found to stimulate hair protein production, which may help with hair growth.

The treatment was ineffective in humans.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

A girl inherited excessive body hair from her mother and grandmother.

Premature hair graying in the face may be influenced by genetics and environment.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

A 17-year-old girl and her brothers have a rare hair condition with long eyelashes, thick eyebrows, and easily pluckable hair.

Five Weimaraners had a milder form of color dilution alopecia causing hair loss and skin issues.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Tiger cubs fed artificial milk lacking certain amino acids developed eye problems and hair loss.

Two teenage brothers had a rare, treatment-resistant form of female-pattern hair loss with unusual scalp changes.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

No clear link between specific gene and hair loss in Mexican brothers.

The review says skin conditions with sterile pustules need more research for better treatments.

A woman developed a severe skin reaction called toxic epidermal necrolysis after taking the antibiotic cephalexin.

A man had a non-cancerous neck tumor related to hair follicles removed with no return of the tumor.

Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.

Eyebrow loss has many causes and requires accurate diagnosis for proper treatment.

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

A family got a fungal infection from a boy who had contact with rabbits, but they all recovered with treatment.

The conclusion suggests a new way to classify bradykinin-mediated angio-oedema based on different causes and its possible link with urticaria, which could improve diagnosis and treatment.