Search

everythinglearnresearchcommunity

for

Search:↓

People with certain allergic conditions or higher white blood cell counts have more severe hair loss, and treating hair and nail side effects early in melanoma therapy can improve quality of life.

New LSS gene variants help understand congenital hypotrichosis 14 better.

A specific gene mutation causes sparse, brittle hair in a family.

Shaving and avoiding brushing improved the patient's beard hair condition.

A hair growth ointment improved hair length in a family with a genetic hair growth condition.

A unique type of hair loss mimics another condition but has minimal inflammation and specific immune cells present.

Isolated patchy heterochromia with pili annulati can occur without other health issues.

The condition is harmless, doesn't worsen, and needs no invasive treatment.

Facial lichen planopilaris may be triggered by shaving and mustard oil, and early detection is crucial for better treatment outcomes.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Ixekizumab may be an effective first treatment for a rare skin condition causing hair loss.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

ILC1-like cells can cause alopecia areata by disrupting hair follicle immunity, suggesting a new treatment approach.

A rare case of severe scalp hair loss and nail issues in keratosis follicularis was observed.

Trichoscopy helps diagnose and track alopecia areata by examining specific hair and scalp markers.

Dermoscopy helps diagnose different hair loss conditions, and characteristics vary among ethnicities and individual cases.

Excessive eyelash growth from erlotinib may indicate positive tumor response and help treat madarosis.

Two boys had a rare skin condition needing to be differentiated from similar disorders, with unclear inheritance due to few cases.

Trichotillomania can be identified by a "Friar Tuck sign" and nail-biting.

Using animal names for skin conditions helps with learning and memory.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Trichoscopy helps distinguish Lichen Planopilaris from Frontal Fibrosing Alopecia by identifying unique hair loss patterns.

Pigtail hair is a sign of new hair growth and should be recognized in hair loss conditions like acute telogen effluvium.

Exclamation mark hairs help distinguish syphilitic alopecia from alopecia areata.

Woman has discoid lupus, frontal fibrosing, and androgenetic alopecia.

A 6-year-old girl was diagnosed with a rare hair disorder called monilethrix.

Hypothyroidism patients with hair loss typically have thinning hair, smaller hair follicles, and normal hair shedding.

Topical minoxidil can help improve hair in trichonodosis.