Search

everythinglearnresearchcommunity

for

Search:↓

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

The research identified genes that explain why some sheep have curly wool and others have straight wool.

Different hair loss types need accurate diagnosis for proper treatment.

Frontal Fibrosing Alopecia might be an autoimmune disease.

The document recommends a team-based approach and personalized care for managing diabetes in teenagers.

Early treatment of acne is crucial to prevent scarring and psychological effects.

Actinic keratosis is a sun-induced skin condition that can potentially turn into skin cancer and requires various treatments to prevent this.

Actinic keratosis is a sun-induced skin condition that can potentially turn into skin cancer and requires treatment to prevent malignancy.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

A child with a rare vitamin D-resistant condition improved with treatment.

Genetic changes in mice help understand skin and hair disorders, aiding treatment development for acne and hair loss.

A mutation in mice causes hair loss and immune problems.

A gene mutation in mice causes permanent hair loss and skin issues.

The scraggly mutation causes hair loss and skin defects in mice.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Mutations in the AR gene cause hair thinning and loss.

New genes linked to male pattern baldness were found on chromosome 20p11.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

A specific gene mutation causes congenital hair loss.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.