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A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Polydopamine is a safe, effective, and permanent hair dye that turns gray hair black in one hour.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

The mineralocorticoid receptor may play a role in skin and hair health and could be a new target for treating related disorders.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

A patient with a rare hair condition and skin disorder showed hair improvement after treatment.

Magnesium supplements improved quality of life for women with polycystic ovary syndrome, but didn't help with acne, hair loss, or abnormal bleeding.

Adding cetirizine to minoxidil improves hair growth and thickness in women with androgenetic alopecia.

Hair changes can indicate systemic diseases or medication effects.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

The book details skin conditions in older adults, their link to mental health, cancer treatment importance, hair loss remedies, and managing autoimmune and itchy skin.

Dr. SKS hair booster serum effectively treats hair loss caused by COVID-19.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

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

A gene called HDAC9 might be a new factor in male-pattern baldness.

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

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Potassium levels affect blood sugar and insulin during dialysis, and malnutrition changes children's hair roots.

HPV genes in mice improve ear tissue healing by speeding up skin growth and repair.

Levetiracetam may cause hair loss, which can potentially reverse with lower doses or stopping the drug.

FUE megasession effectively treats severe hair loss with natural-looking results in one operation.

Up to 50% of scalp hair can be lost before it appears thin, and treatment is only needed for hair loss caused by diseases or deficiencies.

The Yorkshire terrier has a genetic hair loss condition not improved by treatment.

No link found between new male baldness genes and female hair loss.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Short anagen syndrome involves a hair growth phase lasting 1.5 years.

A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.