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A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

Eating vegetarian, having allergies, and family history might be linked to getting gray hair early.

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

PCOS in lean women is a serious health condition with implications beyond fertility, affecting metabolism and increasing cardiovascular disease risk.

The document concludes that there is a need for more research and regulation in dermatology, covering topics like latex allergy in children, the use of botulinum toxin, and treatments for skin conditions.

Hypertrichosis lanuginosa causes excessive fine hair growth, often linked to genetics or cancer, with limited treatment options.

A 15-year-old girl has a benign skin tumor on her neck.

Nilotinib can cause keratosis pilaris, a skin condition.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

A 78-year-old man with Cronkhite-Canada syndrome improved significantly after treatment and remains symptom-free.

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

Brothers of women with PCOS tend to have higher levels of a hormone called DHEAS, indicating a possible genetic link.

A specific gene mutation causes Olmsted syndrome.

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

ESR2 gene linked to female-pattern hair loss.

Keratosis pilaris is a common skin condition where hair follicles get clogged with keratin, mostly on the arms and thighs.

Triptolide effectively and safely reduces actinic keratosis lesions in mice.

Cow milk sugars increase fat production and inflammation in skin oil cells.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

Scientists created a tiny, 3D model of a hair follicle that grows and acts like a real one.

Intravenous calcium therapy is a safe and effective treatment for a rare type of rickets.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

A hair growth ointment improved hair length in a family with a genetic hair growth condition.

Hair loss in androgenetic alopecia is caused by genetic factors and androgen excess, and can be treated with combined therapies.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.