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

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Hidradenitis Suppurativa is a chronic skin condition best treated early with surgery for better outcomes and less recurrence.

A man's unusual scalp folds caused by a skin condition were treated with surgery and remained unchanged two years later.

5-alpha reductase inhibitors may help protect the brain and gut in Parkinson's disease.

Diabetes can lead to blindness and skin problems, and managing blood sugar and blood pressure is crucial to prevent these complications.

The document lists common and scalp-specific lesions, emphasizing the need for hair restoration surgeons to recognize these and refer patients to a dermatologist if necessary.

Notch signaling disruptions can cause various skin diseases.

Dutasteride may help protect neurons and reduce inflammation in Parkinson's disease.

The congress showed that psychological therapy can help skin condition patients, social media affects acne stigma, education improves atopic dermatitis, and patient satisfaction in dermatology is high, especially with good doctor engagement.

A woman with unexplained hair loss was found to have harmless skin tumors and a scarring hair loss condition, but the tumors didn't cause the hair loss.

Hidradenitis suppurativa treatment should be tailored to the individual, with quitting smoking being important.

People with Down's syndrome are more likely to have syringomas.

Skin symptoms can indicate endocrine disorders and have various treatments.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

The conclusion is that hair loss from CCCA may be genetic and not solely caused by hair grooming practices.

Treatment with dutasteride, minoxidil, and artificial hair transplantation improved appearance but caused folliculitis.

Familial factors affect hair loss types in Koreans, with M type in men, L type in women, and paternal factors influencing male hair loss more.

Fish oil improves skin health in people with diabetes and high cholesterol.

The conclusion is that managing cholesterol is important for women, especially during pregnancy, breastfeeding, and with PCOS, and involves regular screening and careful treatment choices.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

The document concludes that detailed clinical descriptions of seven family cases help understand dominant dystrophic epidermolysis bullosa's symptoms and inheritance.

Acne can appear or persist in adulthood due to hormonal changes, external factors, or substance use, and requires appropriate treatment.

Dissecting cellulitis of the scalp is a condition that causes inflammation and scarring on the scalp, mainly affecting African-American men, and can lead to permanent hair loss.