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Generalized trichoepitheliomas with hair loss may indicate myasthenia gravis.

Defective protein folding due to a mutation is key in ANE syndrome.

Basonuclin helps keratinocytes multiply and prevents them from fully maturing.

Patients with a specific genetic variant have more severe alopecia areata and higher recurrence rates.

Brindled mice show abnormal catecholamine neuron development due to copper deficiency.

Genetic factors might cause fibrosing alopecia linked to hair shaft abnormalities.

A new DSG4 gene mutation causes hair defects in a young girl.

Hair-shaft abnormalities can indicate neurological disorders, some of which are treatable.

miR-155-5p can help diagnose and track alopecia areata severity.

Ultrasound biomicroscopy is useful for viewing hair follicles in alopecia areata.

Micronutrient levels and thyroid function likely don't affect scarring alopecias.

The family has a unique form of ectodermal dysplasia similar to Clouston syndrome but with different hair and skin symptoms.

miR-31 regulates hair growth by controlling gene expression in hair follicles.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

LEF1 is essential for the development of airway glands and is regulated by the Wnt/ß-catenin pathway.

Tumid lupus erythematosus can cause non-scarring hair loss on the scalp and requires careful diagnosis.

Mitochondria change shape to meet energy needs during cell movement.

Some family members had a condition with both loose hair and unique eye changes, possibly indicating a new type of ectodermal dysplasia.

Mycophenolate mofetil improved skin condition in a man with nephrogenic fibrosing dermopathy.

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

Trichofolliculoma is a rare skin bump on the face or scalp.

Ponatinib can cause a rare skin reaction that resolves with topical treatment and temporary drug discontinuation.

Mouse zigzag hair bends form due to a 3-day cycle of changes in hair progenitors and their environment.

Two new gene mutations cause a rare hair disorder.

New mutations in the DSG4 gene cause a rare hair condition.

A rare skin growth was successfully removed without recurrence after one year.

Minoxidil use can cause trichostasis spinulosa in long-term hair loss patients.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

c-Myc, Max, and Bin1 help hair follicle cells mature and die.