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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.

A woman with Parry-Romberg syndrome developed new curly hair on one side of her scalp, a condition not previously linked to the syndrome.

Woolly hair is a rare genetic condition with no effective treatments.

Hair transplant surgery can sometimes lead to nerve pain in the face.

COVID-19 may cause hair loss and scalp pain due to inflammation and changes in hair follicle receptors, but these symptoms typically resolve in 2 to 4 months.

A rare, harmless hair condition was found in an infant's eyebrow, needing no treatment.

Some burn patients grew extra hair in areas treated with pressure garments or silicone.

The trichoscopy-assisted hair pull test is useful for diagnosing different types of hair loss.

31% of female high school students in Minia have hair loss from tight hairstyles, which can become permanent if not treated early.

Trichoscopy is a valuable, quick, and non-invasive tool for diagnosing tinea capitis in children.

C-tactile nerves are sensitive to hair movement.

Pili annulati is caused by a protein metabolism disorder affecting hair structure.

Trichoscopy helps tell apart alopecia areata and trichotillomania in Asians by looking at specific hair and scalp features.

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

A dark-haired Chinese girl had hair that looked banded under certain light but was normal under a microscope.

Trichoscopy helps tell apart other hair loss conditions from common hair loss.

Twisted hair is rare in severe anorexia nervosa, found in only 2 out of 30 patients.

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

Fungal infections should be considered in scalp swelling to avoid misdiagnosis.

Scalp inflammation can cause multiple hairs to grow from one follicle.

Trichilemmal carcinoma is a rare skin cancer that requires careful diagnosis and follow-up.

A 23-year-old man has a benign, non-progressive hair loss patch that doesn't respond to treatment but can be cosmetically treated.

UV-enhanced trichoscopy helps diagnose hair shaft disorders like pili annulati.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

Monilethrix causes brittle hair and hair loss, and it runs in families.

A rare hair disorder with multiple hairs from one follicle was found on a patient's abdomen.

Trichoblastomas may mimic fetal skin development by having many Merkel cells, unlike adult skin.

Two sisters with Netherton's syndrome had skin and hair issues, needing special diet and ointments.

Two boys had a rare skin condition needing to be differentiated from similar disorders, with unclear inheritance due to few cases.