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Thyroid function may influence hair loss after COVID-19.

Sweat gland development involves two unique skin cell programs and a temporary skin environment.

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

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

High TSPEAR levels in colorectal cancer predict worse outcomes.

High TSPEAR levels in colorectal cancer predict worse outcomes.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

A Saudi girl was diagnosed with Loose Anagen Hair Syndrome, a rare condition causing easy hair loss without scarring.

Different fish use the same genes to regrow teeth.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

The document is a detailed guide on skin conditions and treatments for dermatologists.

Neurohormones help control skin health and could treat skin disorders.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

Older hair follicle stem cells have a reduced ability to renew themselves, leading to more hair loss.

Both Th1 and Th2 immune responses are increased in alopecia areata, with Th2 response more strongly linked to how severe the disease is.

Activating Nrf2 helps wounds heal faster by increasing hair follicle stem cells.

Topical tofacitinib is effective in promoting hair growth for non-scarring alopecia.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

The document concludes that proper recognition and treatment of skin appendage disorders are important for management.

The April 2016 JEADV issue covered various dermatology topics, including psoriasis, psoriatic arthritis, mTOR inhibitors, autoimmune diseases, photodynamic therapy, viral DNA in skin diseases, chronic hand eczema, and female hair loss.

Certain gene mutations can weaken the skin barrier and, when combined with environmental factors, lead to eczema and severe itching.

An 8-year-old girl had nail and hair issues that improved without specific treatment, but fungal nail infection was hard to cure.

No effective treatment exists to stimulate hair growth in atrichia with papular lesions.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

Mice treatments didn't grow hair, a patient treatment may affect immune response, and people with hair loss often feel anxious or depressed.

Cell death shapes skin stem cell environments, affecting inflammation, repair, and cancer.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.