Search

everythinglearnresearchcommunity

for

Search:↓

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

A young woman with a rare skin cancer was diagnosed late because her symptoms were unusual for the disease.

Some people with lichen planus pigmentosus might later develop frontal fibrosing alopecia.

Human dermal stem cells can become functional skin pigment cells.

Only skin melanocytes, not other types, can color hair in mice.

Early and accurate diagnosis of congenital smooth muscle hamartomas is crucial to distinguish them from other conditions.

Most skin conditions in Down syndrome are benign and involve dry or thickened skin.

Skin lesions help identify TCM syndromes in alopecia areata.

Melanocytes are crucial for skin pigmentation and can affect conditions like melanoma, vitiligo, and albinism, as well as hair color and hearing.

A dermoscope helps accurately tell apart Pityrosporum folliculitis and Acne vulgaris.

Melanoma development can be linked to the breakdown of skin's melanin-producing units.

Most hair loss in captive rhesus macaques is likely due to environmental and behavioral factors.

Treatment reduced cystic lesions but didn't change existing Nevus Comedonicus.

Better diagnostic tools and treatment guidelines are needed for segmental vitiligo and related pigment issues.

Red dots on the upper chest may be an early sign of certain types of hair loss.

The woman has a rare skin condition called follicular Dowling-Degos disease, which has limited treatment options.

An 8-year-old girl with vitiligo developed extra hair growth on her knee after using tacrolimus ointment.

PAON shows skin patterns due to genetic mosaicism.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

A woman with a rare type of dermatomyositis improved with low-dose prednisone and methotrexate.

The case suggests a possible autoimmune link between lichen sclerosus and vitiligo.

Melanocyte stem cells from non-affected skin in vitiligo patients can become functional melanocytes for potential therapy.

Fetal hair follicles have melanocytes with melanosomes at different stages, which are broken down into pigment particles in keratinocytes.

The study found that long-term sun exposure does not significantly affect follicular plugs on the scalp, and the scalp's appearance is unique compared to other body parts.

Thorough history and examination are crucial for diagnosing genetic disorders like juvenile polyposis and hypomelanosis of Ito.

A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

Minoxidil use may cause skin pigmentation loss.

A 15-year-old boy was correctly diagnosed with a rare skin condition after initially being misdiagnosed.

EFFC might be common but underreported.

A patient with a rare hair condition and skin disorder showed hair improvement after treatment.