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Deleting Smad4 and PTEN genes in mice causes rapid, invasive forestomach cancer.

Hair loss from Telogen Effluvium can be managed by treating the underlying cause and may improve with treatments like minoxidil.

Hair keratin treatments can be harmful, potentially causing health issues like skin reactions and cancer.

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

The Yorkshire terrier has a genetic hair loss condition not improved by treatment.

Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

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

COVID-19 may lead to severe skin necrosis without clear underlying causes, as seen in a diabetic patient who required leg amputation.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

Dentists should start preventive treatments early for children with Ichthyosis Vulgaris to avoid dental problems.

High TSPEAR levels in colorectal cancer predict worse outcomes.

High TSPEAR levels in colorectal cancer predict worse outcomes.

Resveratrol improved hormone levels, menstrual cycles, hair loss, and ovarian function in PCOS patients.

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

People with Down syndrome have a higher risk of skin disorders and need better screening and treatment.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

A man with four autoimmune diseases suggests a new category for multiple autoimmune syndrome.

Different fish use the same genes to regrow teeth.

A boy with progeria had eye problems and signs of aging like hair loss and skin wrinkling.

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

A woman's severe hirsutism was caused by Leydig cell tumors in her ovaries, which improved after surgery.

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

Accurate diagnosis and timely, tailored treatments improve outcomes in obstetrics and gynecology.

MRI helps distinguish between pituitary adenomas and craniopharyngiomas, guides treatment for pediatric CNS tumors, and assesses rhinocerebral mucormycosis with a high mortality rate in transplanted patients.

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

Low-level laser therapy effectively reduces the size of pressure ulcers compared to placebo.

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.