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A specific gene mutation causes varying hair loss severity in a Pakistani family.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

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

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

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

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

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

Scalp involvement is common in pemphigus and can lead to hair loss, with the severity of scalp lesions linked to overall disease severity.

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

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.

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

Terbinafine is more effective than itraconazole for toenail fungus, especially in older patients, and debridement improves its effectiveness.

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

Dermoscopy improves diagnosis and treatment monitoring for children's skin infections, inflammations, and hair disorders.

The conclusion is that exogen is a unique hair cycle phase and the new sampling method specifically targets this stage, which may help in future hair loss research.

Smad4 is important for healthy hair follicles because it helps produce a protein needed for hair to stick together and grow.

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

Cats with abnormal hair had DSG4 gene changes causing hair problems.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Desmoglein 4 is controlled by specific proteins that affect hair growth.

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

Hair microscopy is a simple and cost-effective method to help diagnose systemic diseases in children.

Monilethrix causes fragile, patchy hair loss.

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

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

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

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.