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A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Jarilla-Coffea extract gel effectively and safely increases eyelash and eyebrow thickness in women.

Low-dose oral isotretinoin improved hair loss and facial bumps in patients with a specific type of hair loss.

Frontal fibrosing alopecia might be linked to autoimmune diseases.

KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.

Tofacitinib was effective in treating hair loss in two patients with alopecia universalis.

Tofacitinib helped a teenager with severe hair loss grow hair back, but more research is needed.

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

Some patients with a type of skin lymphoma can experience a rare, non-scarring hair loss that looks like another hair loss condition but has distinct features.

A Korean woman with complete hair loss regrew her hair after taking tofacitinib, with no side effects.

Keratosis Pilaris Atrophicans causes skin scarring and might be treated with a new synthetic retinoid.

Most treatments for lichen planopilaris were found to be generally unsatisfactory.

Tofacitinib helped some young children with severe hair loss grow their hair back without bad side effects.

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

Nonhead hair transplantation is effective for patients with limited head donor hair, but more research is needed.

Latanoprost works better for hair growth, and combining it with betamethasone valerate is most effective.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

Follicular Unit Hair Transplantation has become a less invasive procedure with natural results, suitable for certain adults with hair loss.

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

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

A 45-year-old woman with autoimmune diseases experienced patchy hair loss due to alopecia areata, which has no cure but can be treated, with varying success.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

Guidelines for diagnosing common hair loss include detailed history, clinical examination, and various diagnostic techniques.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Cancer patients treated with immune checkpoint inhibitors may develop alopecia, but some hair regrowth is possible with treatment.

The document concludes that early recognition and treatment of primary cicatricial alopecia is crucial to prevent permanent hair loss.

The document concludes that more research is needed to understand excessive hair growth in women with normal hormone levels and regular ovulation.

Certain leukemia drugs can cause severe skin reactions that may require stopping treatment.

A woman's eyelash regrowth was successful using tofacitinib solution for alopecia areata.