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The study found that polymorphous light eruption varies among patients and can be distinguished from benign summer light eruption by the time it takes for symptoms to appear after sun exposure.

The child's hair loss was due to syphilis and improved after penicillin treatment.

Old C57BL/6 mice with unsynchronized hair cycles show less melanin in their spleens.

A patient with a rare chromosome condition also had a rare type of hair loss.

Monilethrix Syndrome causes fragile, beaded hair that breaks easily and needs early diagnosis for better care.

Some people with the skin color loss condition, vitiligo, also develop the skin inflammation condition, lichen planus, possibly due to local trauma, sun damage, or genetic factors.

UV light causes skin color loss in bald areas; wear a cap and use sunscreen.

A young boy with a rare skin and nail condition improved significantly with simple topical treatments.

Epithelial grafting can effectively repigment white hair in vitiligo patients.

The nodule was a benign cutaneous lymphadenoma, not cancer, and was successfully removed.

A man with a skin nodule was diagnosed with a rare skin condition called cutaneous focal mucinosis, which can be confused with other skin cancers.

A 14-year-old boy is the youngest person reported with a rare, benign tumor related to hair follicles, usually found in older people.

Diphencyprone can cause unexpected and possibly permanent vitiligo.

A new mutation in the ST14 gene was found in a patient with ARIH syndrome, showing milder symptoms and no tooth issues.

Genetic hair shaft abnormalities can be seen with microscopes and often affect scalp hair.

Hair color production is closely linked to the active growth phase of hair in mice and may also influence hair growth itself.

Monilethrix is a rare genetic hair disorder that's hard to treat.

Monilethrix, a genetic hair disorder causing fragile hair, affects three generations in a family.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

The document describes previously unreported unique skin changes in a rare genetic disorder called Hereditary mucoepithelial dysplasia.

Hereditary factors cause hair loss in mice by affecting skin and hair follicle structure.

Generalized trichoepitheliomas with hair loss may indicate myasthenia gravis.

Human skin's melanocytes respond to light by changing shape, producing pigments and hormones, which may affect sleep patterns.

Dermoscopy helps doctors recognize a type of benign skin tumor called pilomatricoma.

Minoxidil solution applied twice daily improved hair growth in patients with Woolly Hair/Hypotrichosis due to LIPH gene issues, with mild side effects.

Trichothiodystrophy causes unusual hair and developmental issues.

Two siblings have a rare hair condition caused by a new genetic variant.

Removing a tumor may resolve associated skin and hair symptoms.

Melanin density affects hair color, and this method can help in cosmetic assessments and diagnosing hair diseases.