Search

everythinglearnresearchcommunity

for

Search:↓

Exosomal miR-199a-3p from dermal papilla cells helps control hair color by affecting melanocytes.

PPAR agonists show promise for skin conditions but need more research before being a main treatment.

Topical minoxidil may help treat a rare genetic hair condition with no fully effective treatments yet.

Etanercept may cause lichen planopilaris, so doctors should be cautious.

1,25-dihydroxyvitamin D3 helps melanocyte precursors from hair follicles grow and produce melanin, aiding vitiligo treatment understanding.

Short telomeres may cause symptoms like hair loss and osteoporosis, offering insights into aging.

Targeting pyroptosis may offer new treatments for alopecia areata, but more research is needed.

HAIR may cause fetal loss by triggering different cell death processes in the uterus and placenta.

Keratosis pilaris is a common skin condition where hair follicles get clogged with keratin, mostly on the arms and thighs.

Two enzyme defects in biotin metabolism cause severe skin, hair, and metabolic issues.

Stopping erlotinib improved severe hair loss and skin issues in a patient.

Acitretin treatment unexpectedly darkened a patient's gray hair.

The article concludes that it's important to know how to identify and treat the rare hair disease black piedra, even in places where it's not usually found.

Researchers found a gene mutation responsible for a rare hair loss condition.

Erosive pustular dermatosis of the scalp is a type of skin inflammation often confused with other conditions, requiring continuous treatment.

A rare scalp condition mainly in older women can be treated with various alternatives to steroids, which may have fewer side effects.

Women are more likely to have Lichen planopilaris, and treatments with cyclosporine and methotrexate are most effective but less safe than mycophenolate mofetil.

Iron deficiency in mothers causes hair loss in their baby mice.

Rituximab treatment led to complete hair regrowth and improved skin in a woman with pemphigus foliaceus.

The man has a disease causing skin patches, thickened nerves, and mild muscle weakness.

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

The case shows skin changes can indicate deeper health issues like insulin resistance, which are challenging to manage.

Type 1/17 inflammation in psoriasis increases skin cell growth due to a molecule that could be a new treatment target.

Blocking mTORC1 activity with rapamycin could help increase hair pigmentation and growth, potentially reversing gray hair.

The treatment is a safe and effective option for hair regrowth in patchy alopecia areata.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Knockout mice showed anemia and hair loss, suggesting other ways exist for iron absorption.