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A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

A scalp biopsy revealed systemic amyloidosis in a woman who initially seemed to have a common hair loss condition.

New genetic mutations causing hair loss were found in a Chinese family.

Frontal fibrosing alopecia is a challenging hair loss condition with no known cause or definitive treatment.

Immunological treatment improved both neuropathy and alopecia.

A woman with undifferentiated connective tissue disease was diagnosed with renal amyloidosis and carpal tunnel syndrome.

Bullous lupus can cause severe esophageal issues but responds well to corticosteroids and azathioprine.

Amyloid proteins can cause rare hair loss by depositing in the scalp.

The Oat mouse model shows mild retinal degeneration, useful for testing treatments.

A specific gene mutation causes severe skin and nail issues and hair loss.

Clinicians should recognize taste disorders and hair loss as important symptoms in myasthenia gravis patients.

Agalsidase alfa helps treat Fabry's disease but needs more research for long-term benefits.

A 2-year-old boy has a rare hair disorder causing brittle hair and hair loss, which may improve with age.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

Genetic discoveries are leading to new treatments for alopecia areata.

The study created a mouse model to mimic degenerative diseases for testing tissue repair and new therapies.

OnabotulinumtoxinA is used to treat wrinkles, pain, sweating, hair loss, and more by temporarily paralyzing muscles and affecting pain pathways.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

The study found that Tourette Syndrome may be linked to certain immune system processes and synaptic signaling.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

Men with Addison disease should be screened for X-linked adrenoleukodystrophy if they have hair loss.

A woman's hair loss improved after removing a tumor in her thymus gland, suggesting hair loss can be linked to such tumors even without a specific muscle weakness condition.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Late-onset alopecia areata in Taiwanese patients is more common in women, usually starts at age 57, often involves less than 10% hair loss, and may have a minimal link to thyroid issues.

Anti-CD19 therapy may help treat SLE and NMOSD.

PolyQ repeats in neural proteins evolve together, affecting brain function and disease.

A specific gene mutation causes congenital hair loss.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

Botulinum toxin injections effectively relieve pain from cutaneous leiomyomas.