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Platelet-rich plasma treatment is not very effective for chronic severe alopecia areata.

Telogen effluvium is a common hair loss condition requiring careful diagnosis and treatment.

The most common cause of hair loss in children in Delta Egypt is alopecia areata, especially in rural school-aged kids.

A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

Polycystic ovary syndrome causes high male hormone levels, leading to symptoms like excess hair, acne, and fertility problems.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

Better-designed, long-term studies are needed to optimize treatment for trichotillomania and trichophagia.

Understanding how DHT works is important for diagnosing and treating hormone-related disorders.

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.

Zinc supplements effectively treat inherited zinc deficiency in infants.

Primary idiopathic pseudopelade of Brocq causes gradual, scarring hair loss with no effective treatment.

Cronkhite-Canada syndrome is a rare condition causing gut polyps, hair loss, skin changes, and nail issues, often with a poor outlook.

Long eyelashes in a patient were an unusual sign of systemic lupus erythematosus.

Polycystic Ovary Syndrome (PCOS) affects 6%-15% of women of reproductive age, causing symptoms like acne and hair loss, and increasing the risk of type 2 diabetes and heart disease; it's managed through diet, exercise, and medications like Metformin and hormonal contraceptives.

The document concludes that hirsutism is the main sign for diagnosing hyperandrogenism, which requires a detailed patient history and physical exam.

Three related Persian cats have a rare, likely hereditary skin condition causing hair loss and poor coat quality, with limited treatment options.

Botulinum toxin has potential for treating various skin conditions and improving wound healing.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

The woman's high testosterone levels indicated PCOS, leading to treatment that improved her symptoms.

The document concludes that PCOS in adolescents is complex and requires comprehensive care to manage its symptoms and associated health risks.

Histone demethylases play a key role in the development of many diseases and may be targets for treatment.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

Androgens like testosterone are important hormones for both men and women, made differently in each sex and affecting the body by regulating genes and quick interactions with cell components.

The 2018 ISPAN Meeting emphasized hands-on learning, patient safety, and professional growth in medical aesthetics and reconstructive practices.

The document discusses how to identify and manage common skin conditions in children.

The document concludes that adenosine receptor agonists have potential for treating various conditions, but only a few are approved due to challenges like side effects and the need for selective activation.

The document concludes that various skin conditions have specific treatments, ranging from antihistamines for urticaria to surgery and medication for tumors and chronic skin diseases.

LEKTI is crucial for skin barrier and immune function, affecting conditions like Netherton syndrome and atopic dermatitis.

Early diagnosis and treatment of alopecia in children are crucial for managing physical and psychological impacts.

Minimally invasive glaucoma surgery can effectively manage glaucoma in GAPO syndrome when other treatments fail.