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A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Taking 5α-reductase inhibitors does not significantly increase the risk of breast cancer in men.

Different hair care practices and conditions affect African American hair and scalp health, requiring specialized knowledge for treatment.

The guide explains how to identify and treat children's hair loss, including fungal infections, autoimmune disorders, hairstyle changes, self-correcting conditions, and behavioral therapy for hair-pulling.

Minoxidil use during pregnancy may cause fetal harm.

The document concludes that specific itchy skin diseases during pregnancy have varying fetal risks and treatments, including corticosteroids and other medications.

Genetics and hormones cause hair loss; finasteride treats it safely.

Mothers and newborns with dental fillings had higher mercury in their hair, but getting fillings during pregnancy didn't raise mercury levels further.

Mutations in the KRT85 gene cause hair and nail problems.

Finasteride doesn't raise acute pancreatitis risk.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Mothers and newborns with dental fillings have higher mercury in their hair, but adding fillings during pregnancy doesn't raise mercury levels further.

PrEP for HIV is less effective in transgender women mainly due to low adherence to the treatment.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Hair loss increases with age; alcohol raises risk, more female partners lowers it.

Msx2 and Foxn1 are both crucial for hair growth and health.

Dihydrotestosterone increases the activity of an enzyme in pubic skin cells that converts testosterone to dihydrotestosterone.

Taking 5-α reductase inhibitors for prostate enlargement or hair loss does not significantly raise the risk of erectile dysfunction.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

A boy had unusual synchronized hair growth with short active growth phases, not fitting known hair disorders.

Healthcare providers need better understanding and cultural sensitivity to improve care for transgender patients with kidney failure needing transplants.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Latanoprostene bunod effectively lowers eye pressure and is better tolerated than other glaucoma medications.

Taking Propecia might lead to the development of cataracts.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Newborns' hair shows how much caffeine their mothers drank during pregnancy.

Finasteride, often used for hair loss, can potentially cause cataracts.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.