Search

everythinglearnresearchcommunity

for

Search:↓

A woman with Castleman's disease died from respiratory failure due to bronchiolitis obliterans.

Children with alopecia areata have different trichoscopic features than adults, including more empty follicular openings and pigtail hairs.

Autophagy prevents early aging and maintains lipid and pheromone balance in mouse glands.

Trichoscopy is better than the hair pull test for tracking alopecia areata.

A specific gene mutation causes sparse, brittle hair in a family.

A rare ovarian tumor caused high testosterone and excess hair in a woman, which was resolved after tumor removal.

Mechanical trauma like towel drying can cause knotted hair even in straight hair.

Hair loss in postmenopausal women due to ovarian hyperthecosis is rare, but removing the ovaries can significantly improve the condition.

Accurate diagnosis of rare pilomatrix carcinoma is crucial for effective treatment.

Men with a certain type of hair loss (vertex type AGA) may have higher levels of bad fats (triglycerides) and lower levels of good cholesterol (HDL), suggesting they could be at risk for high fat levels in the blood (hyperlipidemia).

CCCA is a common hair loss condition in African American women, often inherited and influenced by hairstyling, with unique scalp features detectable by special tools.

Loose anagen hair syndrome is caused by structural abnormalities in the hair follicle's inner root sheath.

Drug repositioning offers hope for new, affordable treatments for a genetic skin disorder called ARCI.

A mare had a functional ovary with a tumor containing cartilage and bone.

Alopecia areata is a common autoimmune condition causing varying hair loss, diagnosed by specific patterns of inflammation around hair follicles, with several treatment options available.

IFAP syndrome is a rare genetic disorder causing skin, hair, and eye issues, with limited treatment options.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.

A man with Acrodermatitis continua did not get better with etanercept treatment, and his condition worsened, suggesting treatment effectiveness may vary by genetics and race.

Severe hair loss (androgenetic alopecia) is linked to higher risk of heart disease (cardiovascular atherosclerosis).

Some family members had a condition with both loose hair and unique eye changes, possibly indicating a new type of ectodermal dysplasia.

Haemochromatosis can cause infertility by affecting hormone glands.

Exclamation mark hairs help distinguish syphilitic alopecia from alopecia areata.

Apoptosis contributes to hair loss in androgenetic alopecia.

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

Apoptosis may contribute to hair loss in androgenetic alopecia.

The research found specific signs to diagnose alopecia areata incognito and noted patients generally regrow hair after steroid treatment.

Impaired autophagy may cause hair loss by triggering early catagen.