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Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

Giant axonal neuropathy changes the structure of keratin in human hair.

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

Better nutrition may reduce fecal incontinence in stroke patients by lowering inflammation and improving antioxidant levels.

A baby's toe was severely damaged by a hair tourniquet, leading to bone and tendon damage, but improved after surgery and treatment.

Testosterone affects brain behavior in complex and varied ways.

Human-robot interaction becomes simpler as robots achieve full autonomy in surgery.

Early neurosteroid changes can alter adult brain function and behavior.

Prenatal THC exposure may harm ovarian health and fertility.

Finasteride may help reduce alcohol cravings and related brain activity.

Large-scale reconstructions enhance understanding of vibrissal sensory mapping in the brain.

A rare form of lupus can cause severe nerve damage and other symptoms, but treatment can help.

Drug repurposing shows promise for treating many medical conditions.

Genetic disorders can disrupt mineral and trace element metabolism, affecting health.

VPS13C variants are linked to more severe REM sleep disorder and faster progression to Parkinson's disease.

Skin cells from people with Epidermolysis Bullosa Simplex have abnormally placed and less active mitochondria.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Understanding genes and hormones is crucial for managing male puberty and sex development disorders.

The study found that nerve signals are stronger when there are more connection points, but not necessarily denser, along the nerve's path in the spine.

Netherton's disease causes multiple hair defects.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

Gene therapy with the Math1 gene helped regenerate balance-related cells and improve balance in mice.

A hair tightly wrapped around a toddler's toe caused severe crying and was treated by surgery.

SH-SY5Y cell lysate is effective for diagnosing Satoyoshi syndrome.

Hair-related body dysmorphic disorder is common in hair loss patients and needs early recognition for proper treatment.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Diagnosing and managing children's hair shaft disorders is challenging but essential.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

Sensory neurons and Merkel cells remodel at different rates during normal skin maintenance.

Abnormal scalp whorls can indicate brain development issues but may also be seen in neurologically normal people.