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A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

Human blood can transfer energy to hair follicles through a glass barrier.

Some children and young adults with eyebrow and eyelash hair loss actually have a hair-pulling disorder, often with related psychological issues.

A chromosomal change may cause ectodermal dysplasia and developmental issues in a child.

Neoplasms hide in hair follicles to avoid the immune system.

Areata-like lupus can mimic alopecia areata but is a form of cutaneous lupus erythematosus.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

Connective tissue nevi have distinct features, and reflectance confocal microscopy is useful for early diagnosis.

The assay effectively identifies compounds that affect immune cell activation.

Monilethrix, a genetic hair disorder causing fragile hair, affects three generations in a family.

A small forehead lesion led to the discovery of a significant brain arteriovenous malformation in a young girl.

Recognizing and treating overlap syndrome in connective tissue diseases is crucial.

The report concludes that atypical Brauer nevus is more common in males, present at birth, and often misdiagnosed due to its unusual scalp locations.

A rare skin reaction occurred when a man took paracetamol, causing a new rash in an area already affected by hair loss.

Hair follicle stem cells might help treat traumatic brain injury.

Severe alopecia areata in children can signal future autoimmune issues.

Generalized hair follicle hamartoma can occur with systemic lupus erythematosus.

The document reports the first Brazilian case of a girl with Becker nevus syndrome, characterized by skin changes, breast underdevelopment, and scoliosis.

The technique allowed noninvasive tracking of hair stem cell survival and growth, showing potential for hair loss research.

A specific gene mutation causes different hair defects in Indian monilethrix families.

Iron can be present in hair color changes without overall iron deficiency.

The transgene likely activated an oncogene or interrupted a tumor suppressor gene, causing melanoma in mice.

The method shows how hair lipids form specific patterns and their roles in hair structure.

A woman with myotonic dystrophy had multiple skin tumors on her scalp, suggesting a genetic link.