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

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

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

Using cetirizine on the skin and taking vitamin D can help increase hair growth in children with hair loss from ectodermal dysplasia.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

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

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

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

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

Early and personalized treatment for hair loss in young people is crucial to prevent permanent damage and should include psychological support.

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

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

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."

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 follicles are essential for skin health, aiding in hair growth, wound healing, and immune function.

Accurate diagnosis and tailored treatments are crucial for managing hair loss in humans and animals.

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

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

A mushroom extract might reduce hair loss and liver damage caused by certain chemotherapy drugs in animals.

Alopecia in animals can be hereditary, congenital, or acquired, with treatments and outcomes varying widely.

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

The document is a detailed medical reference on skin and genetic disorders.

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

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

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

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

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

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

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.