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

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.

The symposium concluded that hair growth involves complex processes, including the hair follicle life cycle, the role of the dermal papilla, hair strength, pigmentation, and the impact of diseases and treatments like minoxidil on hair and skin.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

Eating disorders like anorexia and bulimia cause skin problems, and dermatologists can help detect these disorders early for better treatment outcomes.

Ischemic modified albumin could be a new indicator of oxidative stress in people with alopecia areata.

Indian dermatologists recommend treating common hair loss with a balanced diet, stress reduction, mild shampoos, and sometimes minoxidil and supplements.

Telogen Effluvium is a common hair loss condition, particularly in women, with no specific FDA-approved treatment, and recovery can take up to 18 months.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Some skin diseases and their treatments can negatively affect male fertility.

Telogen Effluvium is a common, usually reversible hair loss condition, often improved by removing the trigger and possibly treated with various products, though their effectiveness is uncertain.

Some vitamins and minerals are important for preventing hair loss, but treating hair loss with them without a known deficiency is not proven effective.

Acrodermatitis enteropathica is a rare inherited disorder causing skin issues, diarrhea, and hair loss.

Zinc therapy improved hair health in a girl with acrodermatitis enteropathica.

Increasing isoleucine intake improved skin and health issues in an infant with maple syrup urine disease.

A baby with a rare metabolic disorder developed a rash not cured by zinc alone, likely due to both zinc and amino acid deficiencies.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

AE can have varied symptoms and genetic causes, but zinc therapy helps.

Oral zinc therapy is effective for treating acrodermatitis enteropathica.

Early diagnosis and biotin treatment are crucial for infants with biotinidase deficiency to prevent severe complications.

A 28-year-old man with type 1 diabetes had skin and hair issues due to zinc deficiency.

Acrodermatitis Enteropathica is a rare skin condition treated effectively with zinc supplements, and early diagnosis is key.

Early diagnosis and lifelong zinc supplementation are crucial for treating acrodermatitis enteropathica effectively.

MSUD patients need careful monitoring of amino acids and zinc to prevent severe symptoms.

A baby with maple syrup urine disease improved from skin problems by adjusting his diet to correct amino acid levels.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

A 7-month-old girl with a rare skin disorder died because diagnosis was delayed.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

An infant with a zinc deficiency skin disorder improved with zinc treatment.