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Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

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

The conclusion is that different types of hair loss in dogs and cats can be cosmetic or serious, and affected animals should not be bred.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

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

A baby with a skin condition improved with treatment but developed a rare form of the condition affecting only his trunk.

The twins' condition is unique and doesn't match any known syndromes.

The endocannabinoid system affects oil production and inflammation in skin cells.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

The conclusion is that hirsutism should be diagnosed and treated because it affects quality of life and may signal other health problems.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

The document concludes that changes in eyelashes and eyelid skin can indicate various local and systemic diseases.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

Postmenopausal hyperandrogenism, a condition with symptoms like increased hair growth and acne, is usually caused by PCOS but can also be due to other factors. It's diagnosed by checking testosterone levels and treated either by removing the adrenal tumor or through antiandrogen therapy.

Hair color is determined by melanin and can be affected by genetic conditions like albinism.

Acitretin is effective for severe skin conditions but has significant side effects and requires careful monitoring.

Narrowband UVB therapy significantly improved a child's rare skin condition.

Retinoids are effective for various skin conditions and hair loss but have serious side effects, so low doses are recommended.

A new therapy for a skin blistering condition has not been developed yet.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

A person was born with both a rare hairless condition and a type of birthmark, which is an uncommon combination.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Stem-cell therapy shows promise for skin conditions but needs more research.

Standard treatment for congenital erythropoietic porphyria was ineffective over five years.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

Stress in hair follicle stem cells causes inflammation in a chronic skin condition through a specific immune response pathway.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

Diabetes often causes various skin problems and complications.

The document reports a unique case of woolly hair with a combination of conditions not previously seen together.

Caffeine may help hair growth in hereditary hair loss.