Search

everythinglearnresearchcommunity

for

Search:↓

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

New research is helping develop better treatments for alopecia areata.

The document explains the diagnosis and characteristics of woolly hair nevus and alopecia neoplastica.

Hair transplantation effectively treated a bald patch in an 18-year-old woman with Temporal Triangular Alopecia.

A woman's new seizures were caused by a brain tumor likely linked to her past cancer treatment, and choosing safe seizure medications is important for women who can have children.

Clomipramine may significantly reduce hair-pulling in Trichotillomania, but more research is needed on treatments and early onset cases.

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

A mother and son both had ulcerative colitis and alopecia, suggesting a genetic link in autoimmune disorders and successful treatment with cyclosporine.

ODC transgenic mice can model human hair loss with skin lesions.

Men have more tryptophan in their hair than women, and it increases with age and is higher in darker and grey or white hair.

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

Women with congenital adrenal hyperplasia have lower fertility, but with proper treatment, they can conceive successfully.

Children with short anagen syndrome usually see their hair condition improve as they get older.

CTA is often mistaken for AA but doesn't respond to steroids and may require hair transplantation.

Tissue expanders effectively repair large scalp defects and restore a natural-looking scalp.

A 38-year-old African American woman has a rare condition that prevents her from growing long hair.

Three Iranian men had reddish-brown facial pigmentation with no effective treatment.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

G-CSF effectively treated a teenager's cyclic neutropenia and reduced her symptoms without adverse effects.

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.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

New tools and criteria have been developed to better assess and treat pediatric lupus.

For hair fungal infections, take oral antifungals; for skin and nail infections, use topical antifungals, and keep affected areas cool and dry.

The review found that basal cell carcinomas on the scalp are not more aggressive than those in other locations.

A 17-year-old girl had severe, on-and-off hair loss, likely due to COVID-19. She was treated with Vitamin D3, biotin, and other supplements, and saw some improvement within a month.

An 18-year-old man was diagnosed with a rare genetic disorder causing hair loss, severe light sensitivity, and skin issues.