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Human dental pulp stem cell-conditioned medium, especially from hypoxic conditions, may help treat chemotherapy-induced hair loss and does not increase cancer risk.

A patient with patchy hair loss was successfully treated for Tumid Lupus Erythematosus after other treatments failed.

Hair loss is common in autoimmune diseases and can be an early sign of the condition, often requiring prompt treatment to prevent permanent damage.

Certain KIR genes in Indian SLE patients are linked to disease severity and could be biomarkers.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

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 twins' condition is unique and doesn't match any known syndromes.

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

Some skin disorders might be linked to H. pylori infection, but more research is needed to confirm this.

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 conclusion is that skin, mucous, and eye problems after Stevens-Johnson syndrome and Lyell syndrome significantly affect patients' lives, highlighting the need for comprehensive care and eye check-ups.

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.

Biomedical engineers are crucial for developing better treatments for chronic and autoimmune diseases.

Cyclophosphamide has serious side effects, but long-term follow-up can help manage risks.

Early treatment of mixed connective tissue disease is crucial to prevent severe autoimmune conditions.

A 36-year-old woman with low potassium levels was found to have Cushing disease, and after treatment, her potassium levels normalized.

A woman lost over 80% of her hair due to a condition called telogen effluvium after having COVID-19.

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

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

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

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.

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