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Microbial biosurfactants could be a safer and environmentally friendly alternative to chemical surfactants in cosmetics.

A 70-year-old woman with bronchiectasis developed a rare immune disease due to a bacterial infection, requiring a difficult balance of treatments.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Netherton Syndrome can cause severe skin lesions in rare cases.

Recognizing oral symptoms can help diagnose and treat blood and nutritional diseases early.

Scalp needle mesotherapy can effectively treat hair loss and improve hair growth.

A rare skin disorder, nevus comedonicus, can appear on one side of the body following Blaschko's lines.

Ferulic acid helps stabilize vitamins C and E for better skin protection from the sun, certain compounds may promote hair growth, atopic dermatitis patients have lower skin defense molecules, older men are more likely to get a type of skin cancer, and a substance called relaxin may prevent age-related skin thickening.

Patients with GATA2 deficiency show early skin symptoms that help diagnose the condition.

A man developed a rare scalp disorder, Folliculitis Decalvans, 20 years after hair restoration surgery, and it required long-term antibiotic treatment.

A boy with toxic shock syndrome had severe heart rhythm problems but recovered with treatment.

Laser hair removal is the most requested cosmetic procedure and has become a scientifically-based treatment suitable for all skin types.

Liver transplantation is a viable option for children with propionic acidemia, improving quality of life and diet, but does not remove all risks and long-term brain outcomes are uncertain.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Parathyroid hormones are important for hair growth, but their use in treating hair loss from chemotherapy is still uncertain.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

The medication lopinavir-ritonavir may cause severe hair loss.

Different hair loss types need accurate diagnosis for proper treatment.

Zidovudine may cause hair loss in advanced-stage HIV patients.

The document concludes that treatments for cicatricial alopecia are not well-supported by evidence, but hair transplantation shows more predictable and satisfactory results.

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

Dupilumab may help hair regrowth in some patients with severe atopic dermatitis, but results vary.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Finasteride is effective for male hair loss, teledermatology is accurate and accepted, and cyclosporin helps treat toxic epidermal necrolysis.

The document summarizes medical findings on topics like heart rhythm treatment, sleep apnea therapy, and various health conditions and treatments.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.