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Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Loose anagen hair syndrome, often affecting young girls, can be diagnosed with a hair-pull test and usually gets better on its own, but severe cases may need treatment.

Detailed patient history and physical exams are crucial for diagnosing hair loss.

The X5 Hairlaser might help treat male hair loss, but more research is needed.

Loose Anagen Hair Syndrome is found in black-haired Indian children and is often missed, especially in boys.

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.

Surface-modified nanostructured lipid carriers can improve hair growth treatments.

Herbal hair oil made with natural ingredients helps reduce hair loss, dandruff, and graying.

Loose Anagen Hair syndrome occurs in dark-skinned children and often improves on its own.

Phaeodactylum tricornutum extract helps hair follicle cells grow by activating the ERK1/2 pathway.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

The document concludes that careful evaluation is key to diagnose and treat women with hair loss, with tests for thyroid, iron, and hormones as needed.

The conclusion is that the best approach for treating Female Pattern Hair Loss is a combination of different treatments.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Acupuncture may be a safe and cost-effective treatment for Seborrheic alopecia.

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.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Mutations in the LSS gene cause a rare type of hereditary 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.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

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.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

Monilethrix is a rare genetic hair disorder with no cure, but low-dose oral minoxidil may help.

Mutations in the P2RY5 gene cause hereditary woolly hair.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.