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The document concludes that certain genetic mutations and dietary factors are involved in acne development, and treatments like isotretinoin and diet changes can help manage it.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

The conclusion is that accurate diagnosis of different types of hair loss requires careful examination of tissue samples and understanding of clinical symptoms.

Pregnancy can increase lupus activity, but careful planning and treatment can improve outcomes.

Skin reactions to drugs are common and can be deadly, usually requiring stopping the drug and may be better prevented with genetic testing in the future.

To manage diffuse hair loss, identify the cause, improve nutrition, remove triggers, and use specific treatments like minoxidil or finasteride.

Mutations in the WNT10A gene cause Short Anagen Hair syndrome and increase the risk of male pattern hair loss.

The book is a comprehensive resource on hair disorders, but lacks information on some conditions.

Trichoscopy is a useful tool for diagnosing hair and scalp diseases without needing skin biopsies.

Boxer dogs may have a genetic skin condition that worsens seasonally and can be treated with certain medications.

The document concludes that skin biopsies, genetic and environmental factors, and specific treatments are important in managing cutaneous lupus erythematosus.

Telogen effluvium is a reversible hair loss condition that requires a detailed diagnosis and often resolves on its own.

Personalized medicine in dermatology uses molecular biomarkers to improve diagnosis and treatment but needs further advancements for practical use.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

Some conditions mimic PCOS symptoms and need careful diagnosis to treat potentially serious health issues.

A one-year-old child with a genetic condition had symptoms improved by treating zinc deficiency.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

The document explains the causes, types, diagnosis, and treatments of hair loss, and its psychological impact, especially on women.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

The document concludes that skin and nail changes can indicate various underlying health conditions.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Skin patterns form through molecular signals and genetic factors, affecting healing and dermatology.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

New digital tools are improving the diagnosis and understanding of irreversible hair loss conditions.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Specialized ribosomes affect aging in human skin cells.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.