Search

everythinglearnresearchcommunity

for

Search:↓

Scalp melanomas are more dangerous and likely to recur or cause death than other head and neck melanomas.

A specific gene mutation causes Olmsted syndrome.

Alopecia neoplastica is hair loss from breast cancer spreading to the scalp.

A 17-year-old girl was diagnosed with a rare ovarian tumor, emphasizing the need for fertility preservation and psychosocial care.

BKN-1 antibody targets specific keratin in basal cell epithelioma and normal skin basal cells.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

A rare skin cancer on a man's elbow was successfully treated with surgery, showing no recurrence after one year.

Postmenopausal frontal fibrosing alopecia is a type of hair loss in postmenopausal women that may stop on its own but has no effective treatment.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

A benign tumor on the cheek, called trichoadenoma, should be surgically removed for cosmetic reasons.

HLD10 can include increased body hair and Mongolian spots.

The study suggests that motor neurons created from stem cells of patients with spinal and bulbar muscular atrophy show signs of the disease, including changes in protein levels and cell functions.

FAPD in children may not depend on androgens and should be treated with anti-inflammatory measures and minoxidil.

Topical 5-Fluorouracil can rarely cause nerve damage, especially in people with a certain genetic deficiency.

Folliculotropic mycosis fungoides has unique molecular features and cell interactions that could guide targeted therapy.

Frontal fibrosing alopecia is a challenging hair loss condition with no known cause or definitive treatment.

Monilethrix is linked to a gene cluster on chromosome 12.

Hair loss might be due to nerve issues, treatable with electric stimulation or acupuncture.

Rapunzel syndrome can show vague symptoms and needs long-term psychiatric care to prevent recurrence.

A person with a new mutation in the SCN1A gene developed brain inflammation after COVID-19.

The back of the scalp has more nerve fibers than the front, which may explain why some people feel more sensitivity there.

Giant axonal neuropathy changes the structure of keratin in human hair.

A specific gene mutation causes woolly hair and hair loss.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

Researchers found a new early sign of Frontal Fibrosing Alopecia that could help avoid misdiagnosis.

EF and PXE not closely related.

A rare skin growth in a baby was successfully removed without coming back.

A large scalp tumor was removed from an elderly woman, who was later diagnosed with schizophrenia.

Some skin growths with mucin can form hair follicles and resemble skin cancer, but a special stain can help tell them apart.