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Strong skin creams work well for long-term scalp inflammation in Rapp-Hodgkin Ectodermal Dysplasia.

A 19-month-old Saudi girl had a rare skin condition with no other defects, and her family was unaffected.

Ovarian hyperthecosis should be considered in young women with severe male-like symptoms and can be managed with hormone treatments.

Many hospitalized children with COVID-19 had skin, mouth, or nail changes, with skin rashes being common.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

Custom-designed implants effectively repaired skull damage in most soldiers injured in combat.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Early treatment of traction alopecia can reverse hair loss; prevention involves avoiding tight hairstyles.

A 22-year-old man has alopecia areata, an autoimmune hair loss condition, with various treatments available.

The document concludes that various hair and scalp disorders in children have specific treatments and proper diagnosis is essential.

Two Sikh brothers developed permanent hair loss from wearing turbans tightly, a condition that became apparent after they moved to Austria.

Hair loss in children can be caused by fungal infections, trauma, autoimmune disorders, or stress, and treatments vary depending on the cause.

The patient's long-term hair loss was caused by leukemia treatments and low estrogen levels, worsened by her genetic tendency for hair loss.

Hair-Thread Tourniquet Syndrome is a rare condition where hair or thread tightly wraps around a child's body part, requiring quick treatment to prevent damage.

The document suggests there might be a link between Kawasaki Disease and Alopecia Areata that needs more research.

The girl with autoimmune hair loss might regrow hair within a year, and treatments can help but not prevent recurrence; dermatologist referral and corticosteroids are recommended.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

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

A girl with lupus and trisomy X has a higher risk of bone problems like avascular necrosis and osteoporosis.

Skin problems are common in Bangladesh due to arsenic, prompt treatment of diabetic foot ulcers is crucial, maternal transmission causes most neonatal herpes, treatments for pediatric vasculitis are effective, the chickenpox vaccine works, more frequent UVB therapy helps psoriasis, certain jobs increase hand dermatitis risk, monoclonal antibodies treat psoriasis well, lifestyle affects psoriasis, alefacept improves psoriasis, imiquimod cream partially clears basal cell carcinoma, and iron may not help chronic hair loss.

Fetal cells could improve skin repair with minimal scarring and are a potential ready-to-use solution for tissue engineering.

The document concludes that early recognition and treatment of PCOS in adolescents is crucial for managing symptoms and long-term health risks.

New treatments for lupus show promise, but more research is needed, especially for children.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Picky eating in children is linked to lower zinc levels and various nutritional deficiencies.

Patients often experience long-lasting changes to their hair after stem cell transplants.

Genetic testing for EGFR mutations is crucial in similar cases.

Two newborns with rare skin infections were successfully treated with antifungal cream.

Surgery is not the right treatment for a fungal scalp infection; proper medical treatment is needed.