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Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Zinc is important for growth and health in animals, plants, and humans, and not having enough can cause various problems.

The conclusion is that self-concept, shame, and emotion regulation are key factors in hoarding disorder, body dysmorphic disorder, and trichotillomania, and should be targeted in treatment and research.

Eating Citrullus colocynthis can cause severe intestinal bleeding and damage.

The document concludes that modern photo stories help represent and challenge how breast cancer affects women's identities and societal norms.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

CD44 signaling can help heal wounds without scars.

The new omeprazole nanoemulgel shows promise as a topical treatment for infections.

Most children with epilepsy on antiepileptic drugs experience side effects, especially those on multiple drugs, but these drugs help reduce seizures.

Adult stem cells with Tp63 can form hair and skin cells when placed in new skin, showing they have hidden abilities for skin repair.

Defective repair processes may cause immune activation and inflammation in psoriatic disease.

High calcium levels in hair may indicate early breast cancer.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

Zinc and copper deficiency harms sheep health and normal body functions.

To prevent and treat Hair-thread tourniquet syndrome in infants, keep a close eye on their limbs, manage maternal hair loss, and educate parents and healthcare providers.

The document describes previously unreported unique skin changes in a rare genetic disorder called Hereditary mucoepithelial dysplasia.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

The patient's hair has unique structural differences with alternating bright and dark bands.

Cholesterol may slow cell division and contribute to male pattern baldness.

SIM01 significantly reduced post-COVID symptoms and is safe.

Using extracellular vesicles from stem cells can help hair grow by affecting scalp cells and hair follicles.

Testosterone increases fluid secretion and aquaporin expression in the vas deferens, which is important for male fertility.

Custom-made consent forms for each plastic surgery procedure improve patient understanding and reduce legal issues.

The study found nine new hair protein genes in human hair follicles.

Females are more likely than males to experience long-COVID symptoms and heart issues.

Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

A girl grew extra hair in areas where she had insect bites.