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

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

A patient with a rare hair condition and skin disorder showed hair improvement after treatment.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

The document explains the diagnosis and characteristics of woolly hair nevus and alopecia neoplastica.

Minoxidil can improve hair growth in some patients with woolly hair due to LIPH variants, with varying responses and mild side effects.

A genetic mutation in the LIPH gene causes hair loss and growth defects.

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

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

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

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

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

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 document concludes that unruly hair can be congenital or acquired, often lacks specific treatments, and can be managed with oils and short hairstyles.

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

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

Hair shaft disorders are diagnosed through examination and history, with general care and some treatments offering improvement.

The document concludes that proper diagnosis and management of hair loss in children require a detailed examination and understanding of various hair disorders.

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

Normal hair thickness varies by scalp area and a mix of hair thicknesses is typical in healthy individuals.

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

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

The document explains the genetic causes and characteristics of inherited hair disorders.

Hair examination helps diagnose rare neurological diseases in children.

The document concludes that individualized treatments for hair issues are effective, certain hair changes can indicate neurocutaneous diseases, specific lotions improve skin health, laser hair removal works but needs more study on long-term effects, men's cosmetics are diverse, peeling is effective but can have side effects, and facial pigmentation is often due to overactive skin cells.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.