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Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Monilethrix causes different levels of hair loss in family members.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

A 10-year-old boy was diagnosed with a rare scalp condition causing hair loss and treated with a topical cream.

Diagnosing and managing monilethrix is harder when it occurs with other hair loss conditions.

Diagnosing and managing monilethrix is harder when it occurs with other hair loss conditions.

Nicastrin deficiency may cause skin cell damage and pigmentation disorders in humans, similar to effects seen in fish.

Selenium deficiency can cause skin and hair color loss, muscle weakness, and blood cell changes, but these improve with selenium supplements.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

The protein p21 is more abundant in normal skin cells than in melanoma cells and may help protect against melanoma, with UVB light affecting its levels.

Uncombable hair is inherited dominantly with complete penetrance.

Removing the liver tumor improved the patient's skin condition and hair growth.

Hemoglobin α acts as an antioxidant in skin cells, especially protecting hair follicle stem cells from UV damage.

Finasteride can cause melasma, especially in people with darker skin.

SKH1 hairless mice have identifiable epidermal stem cells with specific markers.

Polythelia pilosa is a type of extra breast tissue with hair and should be classified as such.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

A rare skin condition in a baby showed unusual fat and hair follicle changes.

A 3-year-old girl with skin mast cell buildup and congenital baldness improved with treatment, suggesting a rare link between these conditions.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

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

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

Oral etretinate improved hair length and reduced beading in monilethrix.

Collagen XVII is crucial for preventing hair and pigmentation loss by maintaining melanocyte stem cells.

A rare skin condition in children can look like other diseases.