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A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

CaBP1 and 2 are important for maintaining the activity of calcium channels necessary for hearing in inner ear cells.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Human scalp hair follicles can produce hormones and have a system similar to a brain-body communication network.

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

pdHGF speeds up wound healing and hair growth.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

Hidradenitis suppurativa may be a type of autoinflammatory skin disease linked to gene mutations and immune system issues.

Skin cells and immune cells change in a skin condition called hidradenitis suppurativa, and a certain treatment can improve these changes.

TMPRSS6 is crucial for controlling hepcidin and normal iron absorption.

CD80CD86 deficiency causes hair loss by disrupting regulatory T cells.

Hirsutism is excessive male-pattern hair growth in women, often treated cosmetically or with hormone therapy if contraception is also desired.

A specific gene variant may increase the risk of developing Alopecia Areata.

Certain HLA class II alleles increase or decrease the risk of alopecia areata.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

LHX2 is crucial for development, tissue repair, and preventing diseases.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

Transplanted bone marrow cells actively move, form clusters, and grow after transplantation.

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

UV light helped human hair transplants survive in mice without broad immunosuppression.

Lhx2 helps retinal cells respond to signals for eye development.