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Eyelashes are important for looks and eye protection, and more people are treating sparse eyelashes; more research is needed to understand eyelash biology and improve treatments.

Mutations in the KRT85 gene cause hair and nail problems.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Recent progress has been made in understanding inherited hair and nail disorders.

Acitretin helped improve hand mobility and skin condition in a patient.

A specific gene mutation causes congenital hair loss.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Three related Persian cats have a rare, likely hereditary skin condition causing hair loss and poor coat quality, with limited treatment options.

Some babies are born with alopecia areata, and a treatment with clobetasol propionate can regrow hair in half of the cases.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

Up to 50% of scalp hair can be lost before it appears thin, and treatment is only needed for hair loss caused by diseases or deficiencies.

Congenital Triangular Alopecia is a rare, non-scarring hair loss that can be surgically treated in females for cosmetic reasons.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

Recent hair loss research shows some progress, especially in understanding male pattern baldness, but effective treatments for many types of hair loss are still lacking.

Minoxidil cream can safely treat hair loss in kids with ectodermal dysplasia.

Understanding how acne develops in different diseases could lead to new treatments.

Cholesterol balance is important for hair health, and problems with it can lead to hair loss conditions.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Bimatoprost is safe and effective for improving eyebrow hair.

Early diagnosis and tailored treatments are crucial for managing ichthyosis syndromes with hair abnormalities.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

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

Minoxidil helps treat eyebrow thinning, monilethrix, early hair loss, and shortens chemo-related hair loss.

Hair thinning causes stem cell loss through a process involving Piezo1, calcium, and TNF-α.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.