Search

everythinglearnresearchcommunity

for

Search:↓

A new variant of lichen planopilaris causing diffuse hair thinning was identified.

Hair shaft changes may be linked to CCCA, but their role is unclear.

A 2-year-old boy has a rare hair disorder causing brittle hair and hair loss, which may improve with age.

A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

A woman had a rare skin condition with recurring painful nodules that heal in 6 weeks, often without needing treatment.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

The study found that white hair in vitiligo has specific patterns and structures, which vary with the stage of the disease and may be similar to another hair condition.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

Three dogs with a rare skin condition improved with treatment.

The hair disorder was caused by abnormal protein formation, making hair easily damaged.

A woman has a permanent hair loss condition treated with steroids and new medicines, but hair might not regrow.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

A cat had a rare skin disorder with hair loss and scaling, linked to a suspected tumor.

Cross-linked proteins help maintain the structure of hair, feathers, and hagfish teeth.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

The patient had a severe itchy rash and hair loss in the armpits.

Genetic mutations linked to ectodermal dysplasias and hair loss were identified in Pakistani families.

Localized dystrophic epidermolysis bullosa (DEB) can lead to scarring alopecia, highlighting the need to recognize and address this complication.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

A rare scalp condition was successfully treated with specific medications after 9 months.

New LSS gene variants help understand congenital hypotrichosis 14 better.

The study created hair-bearing skin models that lack a key protein for skin layer attachment, limiting their use for certain skin disease research.

The keratin network in mouse skin changes during cornification and affects the skin's protective barrier.

Eruptive vellus hair cysts likely originate from the infrainfundibulum and sebaceous duct.

Hair loss in autoimmune blistering skin diseases varies and may regrow with disease control.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

A rare skin condition was found in a Labrador retriever outside North America.