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Some horses lose hair without inflammation or itching due to various conditions, and while mainly a cosmetic issue, diagnosis requires examination and biopsies, and breeding is not advised if it's hereditary.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

Targeted therapies for lung cancer are effective but require careful management of side effects to benefit patients.

Understanding hair surface properties is key for effective hair care products.

People with allergies or high eosinophil levels have a higher chance of severe hair loss from alopecia areata, and sudden hair loss can indicate chronic graft-versus-host disease.

Iron-deficiency anemia in pregnancy can cause serious health issues for both mother and baby.

A 10-year-old boy's nail condition is mainly cosmetic and improves over time with treatment.

Hashimoto thyroiditis is an autoimmune disease that can lead to an underactive thyroid and is treated with medication and sometimes diet changes or surgery.

Low vitamin D3 is not linked to different levels of thyroid hormones in people with autoimmune thyroid disease.

Herbal cosmetics are becoming more popular because they are safer, have fewer side effects, and offer health benefits.

Ringworm is a common, contagious fungal infection in dogs that can spread to humans and requires lengthy treatment.

Genetic hair shaft abnormalities can be seen with microscopes and often affect scalp hair.

Three patients suffered severe health issues due to not getting enough vitamins and minerals after weight-loss surgery.

CRPS I is complex, linked to immune and nerve issues, and needs comprehensive treatment.

Trichoscopy is a helpful tool for diagnosing Netherton syndrome.

A specific gene mutation causes Olmsted syndrome.

Tiger tail banding and hair abnormalities are reliable indicators for diagnosing trichothiodystrophy.

An 11-year-old girl's hair loss was caused by a Cladosporium fungal infection, which was cured with itraconazole treatment.

Two sisters had a rare hair condition without other usual symptoms.

TTD symptoms vary widely, requiring thorough evaluations.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

A new DSG4 gene mutation causes hair defects in a young girl.

Erlotinib can cause significant but temporary hair loss in lung cancer patients.

A 6-year-old girl was diagnosed with a rare hair disorder called monilethrix.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

Demodex mites are common in adults and elderly, emerging in children, and require careful diagnosis and treatment.

Hair becomes gray and thin as we age, and while most hair loss in older people is due to genetics, there's a chance for gray hair to regain color under certain conditions.

The mats help heal wounds and support bone growth while controlling infections.

Vitamin B complex improves plastic and cosmetic surgery outcomes by enhancing tissue repair and reducing inflammation.

Australia needs better dermatological guidelines for gender-diverse patients.