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Melanocytes are important for normal body functions and have potential uses in regenerative medicine and disease treatment.

Hidradenitis suppurativa is caused by genetic factors, inflammation, bacteria, hormones, and lifestyle factors like obesity and smoking.

New treatments targeting specific genes show promise for treating keratin disorders.

The document lists various dermatology topics, treatments, and diagnostic methods.

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.

Specific genes influence hair and cashmere growth in Laiwu black goats.

Recognizing specific skin features helps diagnose and manage lupus erythematosus effectively.

The study found key factors in the cause of hidradenitis suppurativa, its link to other diseases, and identified existing drugs that could potentially treat it.

The research confirms that Hidradenitis Suppurativa is characterized by increased inflammation, disrupted skin cell organization, and abnormal metabolic processes.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

Future clinical uses of Intense Pulsed Light (IPL) are likely to grow and become more effective with new advancements and combined treatments.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The document concludes that while white skin, nail, and mucosa diseases increase skin cancer risk, they are generally harmless, especially compared to darker pigmentation conditions.

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

The woman has a rare skin condition called follicular Dowling-Degos disease, which has limited treatment options.

Women with androgenetic alopecia may have higher blood pressure levels.

A woman with Degos disease managed her condition for nine years with medications and had two healthy pregnancies, while a separate finding suggests a possible link between female pattern hair loss and high blood pressure.

A woman with thymoma developed a rare chronic condition similar to graft versus host disease after surgery.

The document concludes that using gadolinium-based contrast agents during MRI can be linked to Nephrogenic Systemic Fibrosis in patients with severe kidney disease.

Francisco Camacho Martinez has made significant contributions to skin and sexually transmitted diseases, developed surgical techniques, but is concerned about patient survival rates and over-specialization in dermatology.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Early detection of specific skin lesions can help identify Birt-Hogg-Dube syndrome and prevent serious complications.

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.

Chemotherapy can cause various skin reactions, with hair loss being the most common, and proper diagnosis and treatment of these reactions are important.

RAPK is a rare skin disorder with pigmented spots, mainly on hands and feet, starting in youth.

The document is a detailed guide on skin conditions and treatments for dermatologists.

Mnemonics with one letter are useful and easy to remember for learning dermatology.

The document concludes that certain mutations may contribute to the inflammation in hidradenitis suppurativa and suggests that targeting TNFα could be a treatment strategy.

Researchers identified genes and proteins that may influence wool thickness in sheep.

A man with skin and hair symptoms improved partially with specific treatment.