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A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Alopecia areata can cause spotty white areas on nails.

A child had a rare case of scarring hair loss with skin disease, which is hard to treat and stressful.

SLE patients experience hair loss similar to telogen effluvium, with hair damage and immune activity at hair follicles.

Monilethrix is a genetic hair disorder affecting hair shape, seen in two brothers.

Dermoscopic examination helps diagnose different types of hair loss conditions by showing specific patterns.

A baby with KID syndrome died from infections and organ failure at 18 months old.

Melanin in black hair protects it from sun damage better than light-brown hair.

Some skin problems can be signs of diabetes or other metabolic diseases and recognizing them can help diagnose and treat these diseases early.

Vitamin D helps protect skin, PSORS1 gene's risk interval for psoriasis is expanded, hair follicles can be generated from mouse cells, and interferon-γ may cause pigmented skin lesions.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

Dermatologists are crucial for managing skin side effects in metastatic melanoma patients using vemurafenib and ipilimumab.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

Tricholemmoma is linked to Cowden syndrome and can be benign or malignant.

Topical ruxolitinib quickly improves non-segmental vitiligo.

A 4-year-old had a rare type of hair loss that may have a good outcome.

The document reports a unique case of woolly hair with a combination of conditions not previously seen together.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

Monilethrix involves multiple genes affecting hair structure, including DSG4 mutations.

Most people with systemic lupus erythematosus have skin problems, and skin symptoms are often the first sign of the disease.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

A 79-year-old man was diagnosed with a rare skin condition called nevus comedonicus on his eyelids.

DM and AA may share a common cause.

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

A mother and daughter with similar hair loss conditions and identical HLA types suggest a genetic link between the conditions.

A man had two rare autoimmune diseases that might be connected.

A young goat with skin issues improved with medication and supplements.

A dog with unusual skin lesions near its tail was successfully treated for a rare form of lupus.