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Recognize and treat hair loss conditions that mimic androgenetic alopecia by identifying warning signs and using proper tools.

Frontal Fibrosing Alopecia's cause is unclear, affects mainly postmenopausal women, and current treatments focus on stopping hair loss rather than regrowth.

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

Transplant patients face higher skin cancer risks due to immunosuppressive therapy, requiring careful skin health monitoring.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

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

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

Genetic defects and UV radiation cause skin damage and aging.

Understanding skin structure and development helps diagnose and treat skin disorders.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Certain gene mutations can weaken the skin barrier and, when combined with environmental factors, lead to eczema and severe itching.

The lotion and shampoo effectively treated scalp seborrheic dermatitis.

The document is a detailed medical reference on skin and genetic disorders.

Topical vitamin D is useful for some skin conditions but not effective for others, and more research is needed.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

Different amounts of daylight affect cashmere growth in goats by changing the activity of certain genes and molecules.

Experts met to improve care for ichthyosis patients in Spain.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

ACBP is crucial for healthy skin in mice.

The paper concludes that the 1982 criteria for diagnosing systemic lupus erythematosus need updating to improve accuracy and involve dermatologists in the process.

A severe medication reaction required long treatment and led to hair loss and thyroid issues.

Some people experience lasting sexual, psychological, and sleep problems after using finasteride or SSRI antidepressants, possibly due to similar underlying causes.

The guidelines advise against using testosterone and DHEA in women for most conditions due to safety and effectiveness concerns, but suggest considering testosterone for postmenopausal women with low sexual desire.

Growth hormone levels affect hair growth and loss, with too much causing excess hair and too little leading to hair loss.

Toxic Epidermal Necrolysis is a rare, serious skin condition that can affect anyone, is more common in women, and may be linked to genetics, with a 20% mortality rate mainly due to sepsis.

The Endocrine Society advised against routine testosterone therapy for women, citing a need for more research on long-term safety and a clear definition of androgen deficiency.

Toxic epidermal necrolysis is a severe skin reaction often linked to drugs, requiring careful medication use and supportive care.

The conclusion is that Erosive Pustular Dermatosis of the Scalp is a rare condition best treated with strong topical steroids and sometimes systemic treatment.

Long COVID causes a wide range of long-lasting symptoms that change over time and are hard to diagnose and treat.