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A gluten-free diet and removing the parathyroid adenoma helped a girl with coeliac disease and high calcium levels start puberty.

Nano-PROTACs could improve drug targeting and delivery by using nanotechnology.

A new mouse mutation causes skin and hair defects due to a gene change.

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

Zinc supplements and diet changes can effectively treat zinc deficiency and prevent complications.

Some hair protein genes evolved early and were adapted for use in hair follicles.

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

Cronkhite-Canada Syndrome often leads to death within 6-18 months.

The POMP gene is active in various goat tissues and affects hair growth, with certain treatments influencing its expression.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Skin can produce blood cells, often due to disease, which might lead to new treatments for skin and blood conditions.

Platelet-rich plasma may help heal injuries.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Papain from papaya may help treat cardiovascular diseases by breaking down fibrin.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

Revertant cell therapy could be a future treatment for Ichthyosis with confetti.

New genetic variants linked to albinism were found in Pakistani families.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

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

Chicken feather gene mutation helps understand human hair disorders.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

ABCD1 gene mutations cause adrenomyeloneuropathy, leading to symptoms like limb weakness and spasticity, with management focusing on rehabilitation and spasticity treatment.

A hepatitis B patient lost hair in patches after starting and stopping a treatment with pegylated interferon alpha2a.

Enzyme typing can reliably characterize human hair.

Blocking certain proteins in mouse skin can reduce and shrink skin tumors.

Early diagnosis and multidisciplinary care are crucial for improving the quality of life in patients with ectodermal dysplasia.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Low PON1 levels may indicate and predict the severity of hair loss.