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The fuzzy gene is crucial for controlling hair growth cycles.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

Finasteride may help reduce tic severity in male Tourette syndrome patients.

A drug helped quickly reduce a movement disorder, experts debated the severity of Raynaud phenomenon, and rapid weight loss was linked to temporary hair loss with good recovery.

A baby boy had two types of temporary hair loss at birth, which might be two forms of newborn hair loss combined.

Merkel cell polyomavirus can infect and persist in skin cells, evading the immune system, but certain treatments can control it.

Isoallopregnanolone may be a safe and effective treatment for reducing tics in a mouse model of Tourette syndrome.

Sensory neuron and Merkel cell changes in the skin happen independently during normal skin maintenance.

Beta-trace protein may help diagnose and predict treatment response in certain nerve disorders.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Netherton Syndrome can cause severe skin lesions in rare cases.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

Biotinidase deficiency has various symptoms and can be treated with biotin supplements.

Functional tests and manual muscle testing effectively assess muscle performance in children with health issues.

Two genetic disorders affect biotin metabolism, causing severe skin, hair, and metabolic issues.

A rare skin condition caused droopy and outward-turning eyelids in a patient.

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

Careful diagnosis and management of MCTD are crucial due to potential severe complications.

Frontalis suspension surgery using autologous fascia lata is effective for treating unilateral congenital ptosis with poor levator function.

Trichotillomania is a condition where people repeatedly pull out their hair, which can be triggered by stress and has various physical signs.

Nail issues are common in alopecia areata patients.

Certain defective glucocorticoid receptor mutants move faster inside cell nuclei and work less effectively.

New treatments for immune disorders caused by FOXN1 deficiency are promising.

A 17-year-old girl and her brothers have a rare hair condition with long eyelashes, thick eyebrows, and easily pluckable hair.

Mitochondrial dysfunction is linked to various skin conditions and could be a target for treatments.

Warming hands improves blood flow in people with systemic sclerosis.

Vitamin D receptor knockout mice have significant motor impairments but no cognitive deficits.

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

The cuneate nucleus has two main neuron types: relay neurons and interneurons.