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A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Certain immune cells may cause hair loss by reacting to stressed hair follicles.

A boy with severe immune deficiency and Epstein-Barr virus died from high-grade B-cell lymphoma.

Adalimumab significantly improved symptoms and quality of life in two patients with Hidradenitis Suppurativa.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

A specific gene mutation causes a severe skin disorder in a family.

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

CDH3-related disease causes worsening eye and hair issues.

The muscle damage was caused by T-cell large granular lymphocytic leukemia, not dermatomyositis.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

Both induced and spontaneous AA lymphocytes can cause alopecia areata in mice.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

A rare case of a transplant patient developing a skin condition linked to HPV-49.

Cells that move well may improve hair loss treatments by entering hair follicles.

A 589 nm laser increases IL-2 and IFN-y gene expression in human T-cells.

Farudodstat may help prevent hair loss in alopecia areata by stopping immune attacks on hair follicles.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

Bullous pemphigoid, intrahepatic cholangiocarcinoma, and alopecia areata may share immune-related causes.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

Monilethrix is linked to a gene cluster on chromosome 12.

CD27 and IL-35 can help diagnose alopecia areata linked to bacterial infections.

TBX3 gene affects pigmentation and marking formation in Dun Mongolian horses.

DHL-HisZnNa may help reduce hair loss from chemotherapy, but more research is needed.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

Trichohyalin may trigger the immune response causing alopecia areata.

A mutation in the KRTHB5 gene causes hair and nail issues.

Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.

New treatments for alopecia areata may target specific immune cells and pathways involved in hair loss.

ILC1-like cells can cause alopecia areata by attacking hair follicles.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.