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

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

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.

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

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Shrinking of oil glands in the skin is a key sign of hair loss linked to TNF inhibitor drugs and may improve if the treatment is stopped.

Genetic defects and UV radiation cause skin damage and aging.

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

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

ALA-PDT is effective and safe for chronic X-ray dermatitis, providing complete or partial remission.

People with pemphigus are more likely to have conditions like hypothyroidism, inflammatory bowel disease, and diabetes.

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

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 document concludes that recognizing and treating cutaneous lupus erythematosus early is crucial for managing the skin and potential systemic symptoms.

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

Skin doctors should know about skin and kidney disease links to prevent serious kidney problems.

The document concludes that various findings in rheumatology offer insights into disease severity, treatment responses, and potential risks in medication, with some limitations due to unspecified participant numbers.

The conference concluded that understanding hair and nail disorders is important, iron deficiency may be linked to hair loss, and while some treatments for skin conditions are effective, they may have risks and high costs.

Gender-specific analysis could improve treatment for childhood systemic lupus erythematosus.

SLE and DM can coexist but are rare and need careful evaluation.

Fever and rash can be early signs of lupus.

A woman with lupus had muscle weakness due to kidney issues and was successfully treated with medication.

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.

The document explains different types of skin lesions and their characteristics, causes, and related conditions.

Lack or blocking of SRD5a, a key component in hormone creation, can lead to conditions like pseudohermaphrodism and affect hair growth, bone mass, muscle strength, and reproductive health. More research is needed on its regulation from fertilization to adulthood.

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