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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.

Minoxidil cream can safely treat hair loss in kids with ectodermal dysplasia.

The review shows how to properly diagnose and treat the loss of eyebrow and eyelash hair.

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

The document concludes that understanding hair biology and recognizing hair conditions are crucial for managing and treating hair loss in children.

Accidentally eating a topical steroid may rarely cause acute generalized pustular psoriasis.

Neurohormones help control skin health and could treat skin disorders.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

The document describes the signs of different common types of hair loss.

Hair shaft disorders, often due to genetics or environment, lack specific treatments but can be managed with gentle hair care and may improve with age or topical treatments.

Steatocystoma multiplex causes recurring skin cysts and needs early recognition for better management.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

The document concludes that an experimental drug may help wound healing in Epidermolysis Bullosa, links Hydroa vacciniforme to EBV, discusses diagnosing hair loss disorders, finds many children with eczema have allergies, reviews the safety of a skin medication in children, notes side effects of a Duchenne's treatment, and identifies a marker for pediatric mastocytosis.

New gene discoveries have improved diagnosis and treatment for skin and hair disorders, but more research is needed to fully understand them.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Assessing newborn scalp hair can reveal important health information.

Understanding drug interactions, side effects, and patient-specific factors is crucial for effective dermatological care.

A thorough skin history and full examination are important for diagnosing and understanding the impact of skin diseases.

A thorough skin history and examination are essential for diagnosing and treating skin conditions effectively.

Hair changes can indicate systemic diseases or medication effects.

The document concludes that changes in eyelashes and eyelid skin can indicate various local and systemic diseases.

In a Tuscan pediatric clinic, 7.19% of children had hair or scalp disorders, with nonscarring alopecia being the most common.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

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.

A woman with breast cancer developed a rare condition causing excessive fine hair growth on her face and body.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

Hormone imbalances can cause specific skin changes, which may help in early detection of endocrine disorders.