Search

everythinglearnresearchcommunity

for

Search:↓

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

A man developed a rash similar to pityriasis rubra pilaris after starting sorafenib for cancer, possibly due to the drug's effect on skin cells.

Tofacitinib shows promise for treating severe alopecia areata with good safety and effectiveness.

A genetic variant in the KRT71 gene may cause loose anagen hair and wooly hair, and symptoms might improve with age.

Satoyoshi Syndrome is hard to diagnose and treat due to its rarity and complex symptoms.

IFAP syndrome is a rare genetic disorder causing skin, hair, and eye issues, with limited treatment options.

Mogamulizumab can cause hair loss and skin rashes.

A 16-year-old girl's skin rash was likely caused by an infection and improved with topical steroids.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

The care model improved timely diagnosis and treatment for psoriasis and psoriatic arthritis.

Genetic testing can help diagnose skin conditions but needs more research for full effectiveness.

A man from Brazil had a rare case of leprosy on his scalp, which improved with treatment.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

Treatment improved symptoms in a woman with HAIR-AN syndrome.

The man had myotonia, which caused delayed hand grip relaxation.

FFA is more common in postmenopausal women, can affect younger women, and may stabilize over time.

A patient had both chronic cutaneous lupus erythematosus and frontal fibrosing alopecia.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Loose anagen hair syndrome in children often resolves on its own.

A patient with a rare scalp condition showed improvement with isotretinoin and other medications.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Skin problems after waxing led to a sarcoidosis diagnosis.

Drug repositioning offers hope for new, affordable treatments for a genetic skin disorder called ARCI.

Early recognition of loose anagen hair syndrome is important to prevent misdiagnosis and unnecessary treatments.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.

A family had a genetic condition causing hair loss on the scalp, passed down through four generations.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

Frontal fibrosing alopecia can sometimes look like syphilitic hair loss.