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Platelet Rich Plasma (PRP) treatment is safe and effective for hair growth in people with androgenic alopecia, and can also help treat bacterial infections.

Some skin problems can be signs of diabetes or other metabolic diseases and recognizing them can help diagnose and treat these diseases early.

European dermatologic treatments focus on lifestyle and psychosocial factors, use diverse methods like baths and climate therapy, and emphasize the importance of diet and supplements for skin health.

New retinoids are effective for various skin conditions and are being developed to have fewer side effects.

The document concludes that early diagnosis and treatment are crucial for managing rare hair loss disorders and that more research is needed to improve treatment strategies.

An adult with a rare skin condition improved with tazarotene treatment.

New genetic discoveries may lead to better treatments for alopecia areata.

The rash resolved after stopping ponatinib.

People with Alopecia Areata often have thyroid problems like Hashimoto thyroiditis and hypothyroidism.

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

Some psychiatric medications can cause reversible hair loss.

The Korean study found that twenty-nail dystrophy mainly affects adults, more often women, and has five distinct types with different clinical progressions.

New biopsy techniques and tools improve alopecia diagnosis, and both too much and too little selenium can cause hair loss.

New treatments for Dissecting cellulitis show promise, but more research is needed to understand the disease and establish a standard treatment plan.

Some psychotropic medications can rarely cause hair loss, and stopping these drugs usually reverses the condition.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

Two boys had a rare skin condition needing to be differentiated from similar disorders, with unclear inheritance due to few cases.

Newborns with ichthyosis need specific care based on their skin type.

Acitretin moderately improved skin and eye issues but not hair loss or light sensitivity in a 3-year-old with IFAP syndrome.

A mother and daughter had severe skin, hair, and eye issues linked to IFAP.

Children with severe ichthyosis and growth failure rarely have nutritional deficiencies or gastrointestinal issues, but may experience chronic dehydration.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

The four patients have a unique type of ichthyosis affecting hair follicles.

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

Balneophototherapy effectively treats ichthyosis linearis circumflexa but may need ongoing treatment due to short remission.

Narrowband UVB therapy significantly improved a child's rare skin condition.

Experts met to improve care for ichthyosis patients in Spain.

A girl with a rare skin condition improved after one month of treatment with acitretin.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.