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Melatonin may help with nerve pain, a hepatitis C drug is effective but has side effects, a treatment for mouth sores works but can cause blood issues, ear reconstruction with an implant is safe, HIV transmission from mother to child in Taiwan is now 0% with treatment, certain blood problems are more common in people with a tongue condition, a gene and being overweight are linked to hair loss in some women, a new technique could reduce radiation for lung nodule patients, a hepatitis treatment may lower cancer recurrence after a procedure, and adding extra screening improves tuberculosis detection in patients with lung infections.

A genetic mutation linked to longer life and less disease was found in the Amish, and a drug is being developed to replicate these benefits.

Mutations in the P2RY5 gene cause hereditary woolly hair.

New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

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

Blood tests can help understand the genetic differences in people with alopecia areata, including how severe it is and if it's inherited.

A specific gene mutation causes Olmsted syndrome.

New drugs for rheumatoid arthritis show improvement but have side effects and are not a cure.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

A gene called BMAL1 plays a role in controlling hair growth.

A genetic marker linked to a type of hair loss was found in most patients studied.

SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.

Ishige sinicola extract helps bone-building cells grow and mature, which could aid in treating osteoporosis.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Mutations in the AR gene cause hair thinning and loss.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

Long-term fluticasone treatment does not harm the immune system in horses with heaves.

Cross-sex hormone treatment in transsexual individuals helps understand how sex hormones affect diseases like heart disease and diabetes.

The composition with carnitine, thioctic acid, and saw palmetto extract may effectively reduce inflammation in hair follicle cells.

Minoxidil may help treat hair loss by reducing inflammation-related gene activity in skin cells.