Search

everythinglearnresearchcommunity

for

Search:↓

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Hair usually grows back 1-3 months after treatment for anagen effluvium, and children with Loose Anagen Hair Syndrome often improve by adolescence.

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

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

Short anagen syndrome involves a hair growth phase lasting 1.5 years.

Retinoids are effective for various skin conditions and hair loss but have serious side effects, so low doses are recommended.

Up to 50% of scalp hair can be lost before it appears thin, and treatment is only needed for hair loss caused by diseases or deficiencies.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

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 new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.

Detailed patient history and physical exams are crucial for diagnosing hair loss.

The document concludes that individuals with a rare genetic disorder linked to the AEBP1 gene may experience a unique type of hair loss and should be monitored for heart issues.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

An 11-year-old girl with Trichotillomania developed a large hairball in her stomach, treated with medication, therapy, and family education.

A woman lost all her hair after mild COVID-19, but it started to regrow after treatment with a specific medication.

A man's sudden hair loss and color change to white was diagnosed as alopecia areata and it improved on its own after six months.

An 11-year-old girl with a hair-pulling disorder had a hairball in her stomach and was treated with medication, therapy, and a team of doctors.

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

The herbal hair oil with natural extracts can improve hair health and reduce dandruff.

Up to half of adult women may experience hair loss, and doctors should use medical history, exams, and tests to find the cause and treat it.

The document concludes that alopecia has various forms, each with specific treatments, but no definitive cure for certain types like CCCA has been proven.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

Obesity and bariatric surgery can cause hair thinning and temporary hair loss due to nutritional deficiencies and stress.

Up to half of women by age 50 experience significant hair loss, with various types and treatments available.

Fibrosing alopecia in a pattern distribution is a hair loss condition often confused with other types, requiring early treatment but usually not resulting in significant hair regrowth.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

People with Collagen VI-related myopathies may often have hair loss and scalp issues.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Gender affects hair and scalp characteristics, with differences in hormone responses, graying patterns, and trace metals.