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The document concludes that parathyroid diseases have a range of clinical features and outcomes, with some conditions being treatable and others having a high risk of mortality.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

The document concludes that while white skin, nail, and mucosa diseases increase skin cancer risk, they are generally harmless, especially compared to darker pigmentation conditions.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

Combining minoxidil and plant extracts improved hair growth in a boy with a rare genetic disorder.

Hair restoration surgery can effectively increase pubic hair density, with patient satisfaction and natural results largely depending on the chosen hair pattern and graft design.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

A new gene variant causes glucocorticoid resistance in a mother and son.

Dermal Papilla Cells grown in 3D and with stem cells better mimic natural hair growth conditions than cells grown in 2D.

Early hair loss in men and women may indicate a higher risk of heart disease and metabolic problems.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

Hormone imbalances can cause specific skin changes, which may help in early detection of endocrine disorders.

Eating a lot of soy might lower the chance of early hair loss in men likely to get it.

Dupilumab helped improve skin and prevent new lesions in a child with a rare immune disorder and severe eczema.

Using old drugs for new uses can help treat rare immune deficiencies.

A 16-year-old boy's arm hair grew more after wearing a splint, but it returned to normal in 8 months.

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

The cause of Frontal Fibrosing Alopecia is unclear, diagnosis involves clinical evaluation and various treatments exist, but their effectiveness is uncertain.

Hair loss in men treated best with early medication or transplant, new treatments researched.

Patients often experience long-lasting changes to their hair after stem cell transplants.

A woman developed rare, unexplained curly hair on her scalp and eyelashes.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

Insulin resistance is linked to PCOS and can lead to other health issues, but treatments like metformin can help manage symptoms.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.