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Older men's scalp damage increases with age and sun exposure, a baby girl in the Philippines has Schimmelpenning syndrome, and thyroid screening is advised for children with hair loss and certain risk factors.

Phototherapy is effective and well-tolerated for treating childhood psoriasis and pityriasis lichenoides chronica.

Chesapeake Bay retrievers' hair loss is likely a breed-specific, hereditary condition linked to abnormal steroid levels and distinct skin changes.

A rare lupus case on the chin was successfully treated with steroids and immunomodulators after accurate diagnosis using advanced imaging techniques.

Two patients with Cronkhite-Canada syndrome achieved remission after treatment.

Early diagnosis of skin conditions linked to rickets is crucial to prevent growth and bone issues.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

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

Treatment with vitamin A did not improve the child's skin condition.

Early diagnosis and treatment of hereditary vitamin D-resistant rickets (HVDRR) are crucial to prevent growth issues and other health problems.

The treatment was not recommended due to limited effectiveness and significant side effects.

A young woman had a rare scalp tumor usually found in older women.

LC-OCT helps accurately diagnose different types of infant hair loss without invasive methods.

Skin tumor regression is helped by retinoic acid signaling blocking Wnt signaling.

A child lost eyelashes on one eyelid after COVID-19, likely due to a temporary hair loss condition.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

A vitamin D receptor mutation causes rickets and affects immune responses.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

LC-OCT is an effective new method for diagnosing classic lichen planopilaris.

Retinoids help treat psoriasis effectively, but they can cause side effects and need more research on safe use with other treatments.

A 6-year-old girl had both monilethrix and trichorrhexis nodosa, causing brittle hair, with minimal improvement from treatment.

Airway issues can occur in Conradi–Hünermann–Happle syndrome and can be managed with minimally invasive procedures.

PAON shows skin patterns due to genetic mosaicism.

Hair repigmentation can indicate malignancy and should be investigated.

A child with a rare type of rickets showed some improvement with high doses of vitamin D, but such conditions often respond poorly to treatment.

ODC transgenic mice can model human hair loss with skin lesions.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

A man with a rare disease experienced late hair whitening and loss, but hair color returned, suggesting a good outlook.

A family got a fungal infection from a boy who had contact with rabbits, but they all recovered with treatment.