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Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

The rash on the infant indicated a serious underlying condition.

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

Hidradenitis Suppurativa is likely an autoinflammatory disease, and better understanding its causes could improve treatments.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

The vitamin D receptor helps maintain hair and bone health even without binding vitamin D.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

Understanding genes and hormones is crucial for managing male puberty and sex development disorders.

Doctors need more training in skin cancer screening, a new treatment is effective for a skin condition, better diagnosis methods for skin cancer are available, hair loss in women may be linked to hormones and cholesterol, certain skin care products might cause hair loss, babies' skin gets weaker after birth, and a gene mutation might be linked to eczema.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A 6-year-old girl was diagnosed with a rare hair disorder called monilethrix.

Genetic testing for cancer risk can lead to early and life-saving treatments in people without symptoms.

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

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Different genes are linked to various types of hair loss.

Researchers discovered potential origins and new treatments for skin cancer, including biomarkers for melanoma and therapies that reduce tumor growth.

Pregnancies in a woman with the Donohue mutation were managed with genetic testing, resulting in three healthy infants.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

The Hairless gene is crucial for healthy skin and hair growth.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

Some skin conditions are associated with other serious diseases, and office microscopy may miss many fungal infections.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

Two mouse mutants have defective hair cuticle cross-linking.

Artemis dysfunction might cause hair loss through telomere shortening.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

BAY 43-9006 helps control kidney cancer growth but doesn't significantly increase overall survival.

Mice that can regenerate tissue have cells that pause in the cell cycle, which is important for healing, similar to axolotls.

Volatile organic compounds can cause inflammation and increase the risk of autoimmune diseases.