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A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

An 8-year-old boy with neurofibromatosis type one also has rare hair and eye disorders.

A man's neck lump was a trichilemmal cyst, not cancer, and should be fully removed due to rare risk of becoming malignant.

A child's scalp infection was caused by a fungus not previously known to do so, but it was successfully treated.

Trichoscopy helps diagnose and manage hair and scalp disorders in children.

The patient was diagnosed with oral lichen sclerosus and needs long-term monitoring.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Cronkhite-Canada syndrome causes chronic diarrhea and has a poor prognosis despite treatment.

Trichoscopy helps diagnose and understand Discoid Lupus Erythematosus on the scalp by identifying specific patterns.

A 6-year-old girl was diagnosed with a rare hair disorder called monilethrix.

Biotin improved hair growth and combability in one child with uncombable hair syndrome.

Trichoscopy helped diagnose and treat a child's fungal scalp infection by spotting specific hair shapes.

The treatment improved facial structure and corrected bite issues in patients.

A five-year-old girl has a harmless, unchanging bald patch on her scalp.

A 78-year-old man with Cronkhite-Canada syndrome improved significantly after treatment and remains symptom-free.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

A multidisciplinary approach is crucial for treating complex cases of Rapunzel syndrome in children.

The four patients have a unique type of ichthyosis affecting hair follicles.

Trichoscopy helped diagnose and cure a child's hair loss caused by a fungal infection.

Rothmund-Thomson syndrome causes skin changes, hair loss, and slightly high lysine and cystine in urine.

A rare scalp infection in a child developed into a kerion with additional skin symptoms.

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

Rothmund-Thomson syndrome type 2 can cause chronic, poorly healing wounds.

Toe Tourniquet Syndrome is often misdiagnosed.

A neck lesion misdiagnosed as benign was later treated successfully with Mohs Micrographic Surgery.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

A new mutation in the ST14 gene was found in a patient with ARIH syndrome, showing milder symptoms and no tooth issues.

Dermoscopy improves diagnosis and treatment planning for trichostasis spinulosa.

Trichotillomania is a hair-pulling disorder needing different treatments than OCD.