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A disease causing skin issues in young adult German short-haired pointers is hereditary, with most affected dogs not responding to treatment.

A boy with Sjogren-Larsson syndrome has skin and muscle symptoms due to a specific enzyme deficiency.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Sheep with chronic Sarcoptes scabiei dermatitis have altered keratin expression in their skin.

Deleting the BRD4 protein in certain skin cells causes hair loss and skin inflammation.

A boy's scalp rash and baldness were cured using oral medication and medicated shampoo.

A cat in Brazil had severe skin issues worsened by improper treatment.

A patient with multiple sclerosis developed skin reactions after Daclizumab treatment, requiring more data on the drug's effects.

43.1% of rabbits in Mosul City had mange, with Sarcoptes scabiei var. cuniculi being the most common.

Dogs with dermatitis show significant skin changes and higher white blood cell counts.

A 5-year-old Akita with a rare skin condition improved significantly after treatment.

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

The study concluded that itching and scaling on the face may be caused by a Demodex mite infection.

The document concludes that a woman has both Frontal Fibrosing Alopecia and Lichen Simplex Chronicus, a previously unreported combination of conditions.

Some treatments can improve skin's defense against damage, but overuse may cause other skin problems.

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

Obesity is linked to various skin problems and may increase the risk of skin cancer.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

Obese people have more skin problems like stretch marks and infections, which get worse with higher obesity levels.

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

Keratin proteins in epithelial cells are dynamic and crucial for cell processes and disease understanding.

Chesapeake Bay retrievers' hair loss is likely a breed-specific, hereditary condition linked to abnormal steroid levels and distinct skin changes.

Permanent hair removal with lasers may cure itchy black hair bristles on the back.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

A 29-year-old man had a jaw plaque diagnosed as follicular mucinosis, linked to nestin-positive hair follicle stem cells.

Weight loss surgery improved several skin conditions in obese patients but often caused hair loss.