Search

everythinglearnresearchcommunity

for

Search:↓

Adding cetirizine to minoxidil improves hair growth and thickness in women with androgenetic alopecia.

Trichoscopy is useful for diagnosing different types of hair loss.

Alopecia areata is a chronic condition causing hair loss, with new treatments targeting the immune system showing promise.

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 article concludes that a thorough diagnosis and treatment plan, including medications, non-invasive methods, or surgery, is important for managing hair loss, with a combination of minoxidil and finasteride being particularly effective.

A person was born with both a rare hairless condition and a type of birthmark, which is an uncommon combination.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The document concludes that the girl's hairlessness is likely inherited from her parents.

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

The EDAR gene mutation leads to thinner and more deformed hair shafts.

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

Indian dermatologists recommend treating common hair loss with a balanced diet, stress reduction, mild shampoos, and sometimes minoxidil and supplements.

Mutations in the KRT85 gene cause hair and nail problems.

Black dots under trichoscopy can appear in different hair and scalp conditions, not just in alopecia areata.

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

Congenital Triangular Alopecia is a rare, non-scarring hair loss that can be surgically treated in females for cosmetic reasons.

Some babies are born with alopecia areata, and a treatment with clobetasol propionate can regrow hair in half of the cases.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

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

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Lack of cystatin M/E causes thin hair and dry skin.

Eyelashes are important for looks and eye protection, and more people are treating sparse eyelashes; more research is needed to understand eyelash biology and improve treatments.

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

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Lipase H is important for hair follicle function and shaping hair fibers.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

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

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