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A 14-year-old girl with a condition that makes her hair easy to pull out also has a hair-pulling disorder, and treatment helped but she relapsed after a year.

A young boy with a rare skin and nail condition improved significantly with simple topical treatments.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

Corkscrew hairs can help diagnose trichotillomania.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

Triangular temporal alopecia can occur in adults and should be correctly identified to prevent misdiagnosis.

Children with trichotillomania often pull hair from their scalp and may have other mental health issues.

Trichodaganomania involves biting one's hair and needs combined psychological and medical treatment.

Habit reversal training effectively treats hair-pulling disorder in both adults and children.

Netherton's syndrome may have a familial link and doesn't always include atopy.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

A 12-year-old boy has a rare, harmless hair loss on his chin with no need for treatment.

Alopecia triangular temporal is a rare condition with unclear causes and treatment, but trichoscopy helps in diagnosis.

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

TCHHL1 is a protein important for hair growth, found in hair follicles.

Congenital triangular alopecia can occur outside the typical fronto-temporal region.

Two patients had a unique form of trichothiodystrophy with reduced high-sulfur proteins in their hair.

Triangular temporal alopecia is a benign hair loss pattern best diagnosed with dermoscopy, with limited treatment options like surgery and hair transplantation.

A girl grew extra hair in areas where she had insect bites.

An 11-year-old girl with compulsive hair pulling was successfully treated with therapy and medication.

FOXN1 duplication can cause excessive hair growth.

Three genes linked to the development of trichilemmal cysts were found.

Half-siblings with a rare skin condition improved with treatment for a fungal infection, but hair loss remained.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

An 8-year-old boy with hair-pulling disorder had a bald patch that was confirmed not to be a fungal infection and was treated with therapy.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

TTD hair is brittle due to fewer sulfur amino acids and unstable disulfide bonds.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.