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Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

Two Australian Poll Hereford calves had severe anaemia, abnormal red blood cells, and skin issues.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

Dermoscopy helped diagnose a rare skin disease which slightly improved with treatment.

Hair loss in Cronkhite-Canada syndrome may be due to an autoimmune response.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

A Shih Tzu with Cushing syndrome developed skin issues and was euthanized after treatment led to neurological problems.

Accurate diagnosis is crucial for effectively treating severe alopecia and related symptoms.

Some skin conditions are associated with other serious diseases, and office microscopy may miss many fungal infections.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

The LMNA mutation affects skin structure even in asymptomatic carriers.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Children with diabetes often have skin problems, which can be better managed with good blood sugar control.

NEMO syndrome and systemic lupus erythematosus are linked in a new disease association.

Dendrobium officinale polysaccharide helps hair growth by activating the WNT signaling pathway.

Early minipulse corticosteroid therapy can effectively treat scalp discoid lupus in children.

A 15-year-old boy's skin and hair condition worsened due to improper treatment, leading to severe health issues.

A 12-year-old boy in rural south India had a rare skin condition causing hair loss and inability to sweat.

Dupilumab can cause unexpected scalp issues, so early symptom recognition is important to avoid hair loss.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

A litter of cats had a hair condition similar to a mouse mutation, leading to hair loss and abnormal hair and skin.

A rare scalp tumor involving two hair follicles was successfully removed with surgery, with no recurrence after 7 months.

A baby with maple syrup urine disease improved from skin problems by adjusting his diet to correct amino acid levels.

Desmoglein 4 is controlled by specific proteins that affect hair growth.

Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.

Giving dihydrotachysterol to mother rats caused skin hardening and bone issues in their babies through milk.

A 13-year-old boy with a rare scalp condition improved significantly with isotretinoin, minoxidil, oral steroids, and antiseptic shampoo.

Early treatment of EPDS can improve outcomes and reduce recurrence risk.