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Dermoscopy helps diagnose and monitor treatment for hair loss from scarring conditions like discoid lupus and lichen planopilaris.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

Autoimmune myopathy may be linked to hair loss and skin depigmentation.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

The girl's regrown brown hair had less of certain pigments than her original black hair.

Trichoscopy is crucial for diagnosing alopecia areata by identifying specific hair features.

Vitamin B12 deficiency can cause darkening of all nails.

Latanoprost eye drops caused excessive cheek hair growth and eyelash whitening in a woman.

Hair thickness differences help diagnose hair loss severity.

Latanoprost eye drops caused excessive hair growth and eyelash whitening in a woman.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Knuckle darkening can be an early sign of vitamin B12 deficiency.

Diphencyprone treatment for alopecia areata can cause vitiligo in some patients.

Trichoscopy helps tell apart scalp lesions in pemphigus vulgaris and pemphigus foliaceus and is useful for choosing biopsy locations.

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

Acne in dark skin is influenced by environmental factors and can lead to hyperpigmentation, with various treatment options available.

Treatment improved some symptoms but not all.

Pregnancy can cause skin changes like pigmentation, stretch marks, and temporary hair loss, which often worry the expectant individual.

Children with darker skin tones can have specific skin conditions that need tailored treatments.

Rothmund-Thomson syndrome causes skin changes, hair loss, and slightly high lysine and cystine in urine.

Alopecia areata is a hair loss condition that often starts before age 30 and can affect various body parts, with unpredictable hair regrowth chances.

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

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Langerhans' cells are not responsible for depigmentation in this mouse model.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

Prolonged use of topical corticosteroids can cause excessive hair growth.

HLD10 can include increased body hair and Mongolian spots.