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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.

The document is a detailed guide on skin conditions and treatments for dermatologists.

IGF-1 may affect hair growth and loss, but more research is needed to confirm effective and safe treatments.

A 72-year-old man was diagnosed with a rare skin form of Rosai-Dorfman disease after years of misdiagnosis.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

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

Assessing newborn scalp hair can reveal important health information.

The document concludes that hair loss in cats is caused by various factors, including allergies, mites, infections, and hormonal issues, with treatments varying accordingly.

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

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

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

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

Alopecia in animals can be hereditary, congenital, or acquired, with treatments and outcomes varying widely.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Early and personalized treatment for hair loss in young people is crucial to prevent permanent damage and should include psychological support.

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

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

Five Weimaraners had a milder form of color dilution alopecia causing hair loss and skin issues.

Early diagnosis and treatment, like topical minoxidil, can prevent hair loss in children.

A young cat had a rare hair condition with twisted hair shafts but stayed healthy.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Trichoscopy is a useful non-invasive method for diagnosing different hair loss conditions.