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The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

A mother and son both had ulcerative colitis and alopecia, suggesting a genetic link in autoimmune disorders and successful treatment with cyclosporine.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Telogen Effluvium is a condition causing excessive hair loss due to stress, illness, drugs, or hormonal changes, and can be treated with specific products or naturally resolves after 3-4 years.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

μ-Crystallin may help hair growth by affecting thyroid hormone levels in mouse hair follicles.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

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

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

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

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

The health of the sentinel lymph node is the best indicator of survival for patients with thick skin cancer.

New genetic mutations linked to rare skin disorders were found in three newborns.

Dermatoscopy is a useful tool for diagnosing hair disorders and can help choose samples for more detailed analysis.

Men with Frontal fibrosing alopecia typically lose hair on the front scalp and sometimes on sideburns and upper lip, with treatments showing varied success.

3% topical minoxidil effectively treats extensive alopecia areata with few side effects.

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.

Researchers found a gene mutation responsible for a rare hair loss condition.

A 21-year-old male with a rare genetic disorder experienced sudden hair loss and high DHEAS levels, likely due to a condition similar to PCOS, usually seen in women.

Monilethrix is a rare, inherited condition causing fragile hair and hair loss, with no cure but some treatments may help.

The girl has both monilethrix and Type 1 diabetes, but no link between the two conditions is known.

Low-dose acitretin helps nail psoriasis, stem cells may treat scarring alopecia, Chinese men have lower baldness rates, lateral foldplasty is good for ingrown toenails, hair diameter helps diagnose female baldness, childhood trauma linked to alopecia areata, certain hair-weaving leads to scalp conditions in African American women, and new methods for hair research and understanding hair and sweat gland development were introduced.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Hair transplantation between identical twins can successfully treat severe, nonprogressive hair loss due to follicular aplasia.

Oral minoxidil and growth factors improved hair density and thickness in a girl with hereditary hair loss.

Syphilis can cause hair loss and treating the infection can reverse it.