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Hair loss can cause stress and mental health issues, so treatments should address both the physical and psychological aspects, involving a team of dermatologists, psychologists, and hair specialists.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

DFMO treatment improves hair growth, muscle tone, and development in Bachmann-Bupp syndrome patients.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

A five-month-old boy with Omenn syndrome successfully recovered after a stem cell transplant with reduced intensity conditioning.

A Thai boy was diagnosed with a rare hair disorder causing hair thinning and shedding.

Terbinafine can cause hair loss.

Seborrheic dermatitis is influenced by diet, genetics, and psychological factors.

Women experience various skin issues at different life stages, requiring careful treatment and awareness.

Loose Anagen Hair Syndrome is found in black-haired Indian children and is often missed, especially in boys.

The document concludes that recognizing and treating cutaneous lupus erythematosus early is crucial for managing the skin and potential systemic symptoms.

Some skin diseases and their treatments can negatively affect male fertility.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

The document concludes that proper recognition and treatment of skin appendage disorders are important for management.

Vitamin D supplements may reduce hair-pulling in people with Trichotillomania.

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

New genetic mutations linked to rare skin disorders were found in three newborns.

A 4-year-old girl was diagnosed with trichotillomania, a condition where she pulls out her hair, which may resolve on its own or require therapy.

The document concludes that proper diagnosis and treatment of nonscarring alopecias can improve quality of life and hair regrowth is possible as the hair follicle remains intact.

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

Female pattern hair loss is caused by multiple factors and while treatments like topical minoxidil, hormone therapy, and low-level light therapy can help, none can fully cure it.

The most common causes of hair loss in children in South-East Nigeria are fungal infections and alopecia areata.

New chemotherapy drugs cause skin side effects, but treatments like minocycline and tetracycline can help reduce them.

Lichen planopilaris and frontal fibrosing alopecia are likely the same disease with different clinical appearances.

Alopecia areata treatment varies, with no optimal method established yet.

The document concludes that proper diagnosis and a combination of medical, hair-care, and surgical treatments are important for managing alopecia in black women.

Current research explores hair growth drugs, while future research aims for personalized treatments.