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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.

Amputation stump skin disease worsens life quality, especially in men during summer, and long prosthesis use increases fungal infection risk.

Two cases of hairy elbows syndrome were described, with normal skin texture and symmetrical hair growth.

Hydra can help understand human hair follicle microbiomes and develop new skin disease therapies.

Tofacitinib effectively treated a woman's complex autoimmune and autoinflammatory disorders.

A young woman had a rare scalp tumor usually found in older women.

Tinea capitis should be considered for scalp infections in infants.

Some cases of tinea capitis, a fungal scalp infection, can look like scarring hair loss due to the body's immune response and the fungus itself.

A 7-year-old girl with non-scarring alopecia will have hair follicle transplantation to improve her quality of life.

Actin and alpha-smooth muscle actin help skin heal in mouse fetuses.

Upper eyelid hyperpigmentation can help diagnose facial lichen planus pigmentosus in patients with frontal fibrosing alopecia.

A specific gene mutation causes long hair in Angora rabbits.

Decreased IGF-1R expression may contribute to sacrococcygeal pilonidal sinus development.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Dermoscopy can non-invasively detect eruptive vellus hair cysts on the labia majora.

Trichofolliculoma, a rare benign hair follicle tumor, can potentially recur.

Clinical signs don't match inflammation levels in lichen planopilaris and frontal fibrosing alopecia.

A newborn girl has a rare skin condition with two ulcers on her buttock that are healing on their own.

Pityriasis amiantacea is likely linked to eczema-related skin changes.

Trichostasis spinulosa can be diagnosed with a simple skin biopsy and treated with specific gels, but lesions may return after stopping treatment.

Two sisters with lipoedematous scalp suggest a genetic influence in the condition.

Pili annulati is caused by a protein metabolism disorder affecting hair structure.

The study found that hair follicles are above muscle connections in the scalp, which may help protect stem cell areas.

Human growth factor 20 can boost mouse whisker growth.

A genetic variant in goats is linked to cashmere growth.

Collagenous gastritis is a rare condition causing chronic diarrhea and weight loss, often misdiagnosed due to nonspecific symptoms.

Amitraz effectively treated ferrets with demodicosis without side effects.

The dual-wavelength laser system effectively reduces EFFC symptoms with minimal side effects.

Naevoid bundle hair is an unusual hair growth pattern where multiple hairs fuse together.