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A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

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

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

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

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

Hair microscopy is useful for diagnosing certain hair loss conditions but has limitations and must be interpreted carefully.

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

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

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

Children with short anagen syndrome usually see their hair condition improve as they get older.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

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

Hair diseases can have psychological effects and should be treated with a combination of psychosomatic care, therapy, and medication.

A woman's hair changed to a dry, tangled texture that's hard to comb after treatment with spironolactone, suggesting the medication might cause such hair changes.

Proper diagnosis and treatment of hair loss in children are crucial to prevent lasting issues and maintain their quality of life.

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

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

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.

The document concludes that non-endocrine alopecia in pets varies in treatment effectiveness and often has a poor prognosis, especially in cats.

Hair loss from Telogen Effluvium usually gets better within 6 months after addressing the cause.

Trichoscopy is good for diagnosing and monitoring hair and scalp problems in children but needs more research for certain conditions.