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A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

New genetic mutations causing hair loss were found in a Chinese family.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

A 68-year-old man improved after being correctly diagnosed and treated for a skin condition caused by mites, following a stem cell transplant.

No effective treatment exists to stimulate hair growth in atrichia with papular lesions.

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

EVG staining is a valuable, simple, and cost-effective method for diagnosing various skin conditions in dermatopathology.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

A man with scalp and neck skin issues improved after a year of oral isotretinoin.

A baby had a rare condition with abnormal blood vessels in the brain and unusual skin and hair growth, possibly a new syndrome.

New treatment with green tea polyphenols and nicotinamide improves skin problems from cancer therapy.

A rare scalp condition causing hair loss improved with a specific cream.

COVID-19 can cause various skin issues, with some linked to how severe the illness is.

Tinea capitis can rarely cause urticarial skin reactions in children.

The 1891 epidemic skin disease was likely caused by arsenic poisoning, possibly from beer or fish.

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

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

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

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

Six genetic conditions are often linked to complete scalp hair loss in children.

An infant with complete hair loss was diagnosed with a genetic disorder affecting hair growth.

The Hairless gene is crucial for healthy skin and hair growth.

A man had an allergic reaction to minoxidil, which stopped after he discontinued use and started corticosteroids.

The woman has a rare skin condition called follicular Dowling-Degos disease, which has limited treatment options.

Reducing immunosuppression and using antiviral creams improved the woman's skin condition.

EGFR inhibitors can cause yellowish skin eruptions.

COVID-19 can cause various skin symptoms that usually improve with proper treatment.

The term "Porokeratotic Adnexal Ostial Nevus" is suggested as a more appropriate name.

Methotrexate caused a rare skin rash in a rheumatoid arthritis patient, which resolved after stopping the drug.