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Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

PRP is beneficial for hair restoration.

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

ATP6AP1‐CDG can cause hearing loss, hair loss, and protein issues, even in female carriers.

Green tea compound EGCG could potentially treat colorectal cancer by removing iron and causing stress in cancer cells leading to their death.

Ripretinib is effective and safe for treating advanced GIST in Chinese patients, particularly for non-gastric GISTs.

A specific gene mutation causes a severe skin disorder in a family.

Dracorhodin perchlorate helps heal wounds in diabetic rats by reducing inflammation.

Ritlecitinib is being tested for safety and effectiveness in young children with severe alopecia areata.

Certain gene variations are linked to better memory in healthy Chinese women.

There's a red birthmark on the scalp.

In Japan, sex reassignment surgery for gender identity disorder faces challenges and needs better medical support and education.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Tedisamil and glibenclamide affect cromakalim and minoxidil sulphate differently in rat aorta.

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Few dermatology programs mention gender-affirming care, highlighting a need for better training and visibility.

The CuCS/Cur wound dressing helps regenerate nerves and heal deep skin burns by rebuilding hair follicles.

circCFAP20DC helps goat ovarian cells grow, aiding follicle development.

The hydrogel patch helps heal diabetic wounds by releasing a healing agent in response to harmful molecules and improving skin regeneration.

A new method was developed to measure and assess the activity and inhibition of the enzyme steroid 5α-reductase.

Platelet-rich plasma mesotherapy improved symptoms in patients with corticosteroid-induced rosacea-like dermatitis.

C.I. Acid Orange 3 caused cancer in female rats but not in male rats or mice.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

CCCA may involve the PD1/PDL1 pathway and increased caspase 3, leading to permanent hair loss.

ALRN-6924 can protect hair follicles from chemotherapy damage by temporarily stopping cell division.