Search

everythinglearnresearchcommunity

for

Search:↓

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

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Different hair growth problems are caused by genetic issues or changes in hair growth cycles, and new treatments are being developed.

Disrupted stem cell signals in hairpoor mice cause hair loss.

Different genes are linked to various types of hair loss.

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

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.

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.

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

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Hair follicle stem cells in hairpoor mice are disrupted, causing hair loss.

Photodynamic therapy may not work for erythroplasia of Queyrat and could lead to invasive squamous cell carcinoma.

Hair disorders are caused by a complex mix of biology, genetics, hormones, and environmental factors, affecting hair growth and leading to conditions like alopecia.

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 review concludes that accurate diagnosis of different types of hair loss requires proper biopsy techniques and understanding the hair growth cycle and underlying causes.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

Early diagnosis and treatment, like topical minoxidil, can prevent hair loss in children.

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

Hair ages and thins due to factors like inflammation and stress, and treatments like antioxidants and hormones might improve hair health.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Histone demethylases play a key role in the development of many diseases and may be targets for treatment.

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

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

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

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.