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Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

A protein called lfTSLP is important in causing allergic and other skin diseases and could be a target for treatment.

A 2-year-old girl had a hair disorder not shared by her identical twin.

A specific genetic deletion in goats affects cashmere yield and thickness.

RORA affects hair follicle stem cells' structure and movement, potentially helping treat hair loss.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

Lichen planopilaris can be triggered by prolonged scalp traction and can be treated with corticosteroids.

Dermatologists should consider congenital syndromes like TRPS in young adults with early hair loss.

TRIV-509 quickly improves skin barrier and cell health in atopic dermatitis.

Mouse touch-sensitive nerve cells adjust their connections based on competition with other similar cells.

A girl had rickets due to a gene mutation affecting vitamin D response.

SPARC likely aids in tissue remodeling during the hair cycle, not in starting new hair growth phases.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

The long-pulse alexandrite laser effectively removes hair permanently.

Hairless protein reduces Msx2 gene activity, affecting hair follicle development.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Ritlecitinib effectively promotes hair regrowth in alopecia areata patients, even with extensive hair loss.

Low-dose Ritlecitinib may help children with stubborn Alopecia Areata.

Lichen planopilaris is a common cause of scarring hair loss in Iraq.

An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

Basement membrane changes in lichen planopilaris cause scarring and permanent hair loss.

Removing both KLK5 and KLK7 proteins can prevent death and skin issues in Netherton syndrome.

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

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

Continued ritlecitinib treatment can lead to hair regrowth in some patients with alopecia areata who initially don't respond.

A neglected leprosy treatment led to rare scalp hair loss in an Indian woman, which improved with proper medication.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

Ritlecitinib was generally well tolerated in children with alopecia areata.

Ritlecitinib is being tested for safety and effectiveness in young children with severe alopecia areata.