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A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Stem cells in hair follicles can become various cell types, including neurons.

Naevoid bundle hair is an unusual hair growth pattern where multiple hairs fuse together.

Seborrheic keratosis is a common, harmless skin growth that can look like cancer, so it may need a biopsy.

Neurotrophins are important for hair growth and could help treat hair loss.

Recognizing bamboo hair helps diagnose Netherton’s syndrome.

A man's scalp hair loss was due to a combined melanocytic nevus and alopecia areata, suggesting a possible link between the two conditions.

Halo Scalp Ring is a rare newborn hair loss that can be missed, and early diagnosis can avoid extra tests and worry for parents.

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

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Fahr syndrome causes brain calcification and is managed by treating symptoms and underlying issues.

A rare eyelid tumor was successfully diagnosed and removed, highlighting the need for careful examination.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

The hair defect is due to abnormal inner root sheath keratinization.

Trichoblastoma in the breast can be mistaken for cancer, so expert review is crucial to avoid misdiagnosis.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

A woman's excessive hair growth was caused by a rare benign tumor in her adrenal gland, which was successfully removed.

A rare skin condition with cysts was found on a 5-year-old boy's scalp.

Netherton syndrome causes specific skin and hair changes that help in early diagnosis.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

A rare ovarian tumor caused early puberty signs in a 1-year-old girl, but surgery reduced hormone levels.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

A rare skin condition in a baby showed unusual fat and hair follicle changes.

A rare adrenal gland tumor can cause unusual symptoms due to hormone changes.

Researchers found that hair follicle stem cells can become squamous cell carcinoma due to Ras activation, which could lead to new treatments.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

A 3-year-old boy was diagnosed with a rare, non-scarring hair loss condition called temporal triangular alopecia.

Histopathological examination is crucial to avoid misdiagnosis and ensure proper treatment for skin lesions.

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

Hair casts, also called pseudonits, are often mistaken for other conditions.