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Genetic differences between young and old Tan sheep explain why their fleece changes from curly to straight as they age.

The document is a detailed guide on skin conditions and treatments for dermatologists.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

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

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

The document concludes that understanding hair follicles requires more research using computational methods and an integrative approach, considering the current limitations in hair treatment products.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

Hair examination helps diagnose rare neurological diseases in children.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Lipase H is important for hair follicle function and shaping hair fibers.

New treatments targeting specific genes show promise for treating keratin disorders.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

Too much zinc in the diet can cause hair loss and color change in young mice by reducing copper in the body.

Genes related to calcium signaling and lipid metabolism are important for curly hair in Mangalitza pigs.

Eyebrow loss has many causes and requires accurate diagnosis for proper treatment.

Certain gene variants can cause inherited hair diseases, which are important to diagnose and understand for patient care.

Temporal triangular alopecia is a non-scarring hair loss in children, often linked to other health conditions.

A gene mutation causes woolly hair in a Syrian patient.

Using minoxidil and tretinoin on the skin, along with oral vitamin D, improved hair thickness and density in two girls with woolly hair.

The boy with woolly hair nevus had thinner hair and abnormal hair follicles, which improved with treatment but worsened when treatment stopped.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

A woman with Parry-Romberg syndrome developed new curly hair on one side of her scalp, a condition not previously linked to the syndrome.

Loose Anagen Syndrome causes easy-to-pull, thin hair, mainly in young girls, and improves with age.

The research identified genes that explain why some sheep have curly wool and others have straight wool.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

Minoxidil solution applied twice daily improved hair growth in patients with Woolly Hair/Hypotrichosis due to LIPH gene issues, with mild side effects.