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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 patient with alopecia areata regrew hair after taking tofacitinib and showed changes in certain blood and skin markers.

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

The study found that pili bifurcati causes hair to intermittently split into two branches, each with its own outer layer.

The document explains hair growth, hair loss types, and other hair-related terms.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

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

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

A young woman's Cronkhite-Canada syndrome improved on its own after she gave birth.

Hodgkin's lymphoma can show up as hair loss.

The document concludes that treating female hair loss should target reducing excess androgen and blocking its effects on hair follicles, with the best treatments being hormonal therapy, adrenal suppression, and topical minoxidil.

Hair loss in Cronkhite-Canada syndrome may be due to an autoimmune response.

A young woman developed a bowel obstruction from eating hair from her weave to relieve anxiety.

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

Targeted cancer therapies have a significant but lower risk of causing hair loss compared to chemotherapy.

Lupus can affect the scalp and nails, often causing hair loss and nail damage, and needs early aggressive treatment to prevent permanent damage.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

A woman's hair changed to a dry, tangled texture that's hard to comb after treatment with spironolactone, suggesting the medication might cause such hair changes.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Isolated patchy heterochromia with pili annulati can occur without other health issues.

A 6-year-old girl with alopecia universalis regrew most of her hair after treatment with simvastatin/ezetimibe, minoxidil, and prednisolone.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

Higher IL-17A levels indicate more severe alopecia areata.

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

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

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

The most common causes of hair loss in Jordanian children are fungal infections, autoimmune hair loss, and hair shedding after fever, with zinc deficiency also being a notable cause.