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The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Some skin diseases and their treatments can negatively affect male fertility.

Retinoids can prevent skin cancer in high-risk people but have side effects and require more research on dosing and effectiveness.

Using 5% topical minoxidil improved and normalized the hair growth in a girl with short anagen hair naevus.

The review shows how to properly diagnose and treat the loss of eyebrow and eyelash hair.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

Injecting platelet-rich plasma under the skin significantly improves hair growth and quality without harmful effects.

The guide helps doctors diagnose hair problems by suggesting a thorough patient history, physical exams, and various diagnostic tools.

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

The document concludes that proper recognition and treatment of skin appendage disorders are important for management.

The research found that people's hair proteins vary, especially by ethnicity and body part, which could help identify individuals in forensic science.

The research found that people's hair proteins vary by individual and body part, with some differences between ethnic groups, which could help in forensics.

Abnormal gene expression related to keratin causes hair loss in certain mice.

sPLA2-X is crucial for normal hair growth and follicle health.

A gene mutation in Lama3 is linked to a common type of hair loss.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

A specific gene mutation causes congenital hair loss.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Primary cicatricial alopecia, a rare disorder causing permanent hair loss, is hard to diagnose and treat, with treatments like anti-inflammatory drugs and steroids offering varied results and no guaranteed cure. Psychological support for patients is important, and future research should aim to identify causes of the condition.

B6.Cg-Tyr c−2J Hr hr /J mice have a stronger delayed sunburn reaction and are good for UV research.

Experts met to improve care for ichthyosis patients in Spain.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Six genetic conditions are often linked to complete scalp hair loss in children.

Hair shaft disorders, often due to genetics or environment, lack specific treatments but can be managed with gentle hair care and may improve with age or topical treatments.

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

The document explains how to identify different hair problems using a microscope.